ID

37562

Descripción

Study ID: 104864/902 Clinical Study ID: 104864/902 Study Title: An Open-Label, Single-Arm, Phase II Study of IV Weekly (Days 1 and 8 Every 21 Days) HYCAMTIN in Combination With Carboplatin (Day 1 Every 21 Days) as Second-Line Therapy in Subjects With Potentially Platinum-Sensitive Relapsed Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00316173 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: topotecan Trade Name: CARBOPLATIN Study Indication: Ovarian Cancer; Neoplasms, Ovarian

Palabras clave

Versiones (1)
  1. 7/8/19 7/8/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

7 de agosto de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

HYCAMTIN in Combination With Carboplatin in Subjects with Ovarian Cancer; NCT00316173

Inglés

Investigational Product - IV Dosing

1 formularios  
Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Descripción

Clinical Trial Subject Unique Identifier

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
Investigational Product - IV Dosing (Hycamtin)
Descripción

Investigational Product - IV Dosing (Hycamtin)

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
Cycle Number
Descripción

Experimental drug, Dosage, chemotherapeutics regimen status cycle number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C2045829
Day
Descripción

Experimental drug, Dosage, Day

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0439228
Infusion Start Date
Descripción

Experimental drug, Dosage, Start Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0808070
Infusion Start Time
Descripción

Experimental drug, Dosage, Start Time

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1301880
Infusion Stop Date
Descripción

Experimental drug, Dosage, End Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0806020
Infusion Stop Time
Descripción

Experimental drug, Dosage, End Time

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1522314
Dose
Descripción

Experimental drug, Dosage

Tipo de datos

integer

Unidades de medida
  • mg/m2
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
mg/m2
Actual Dose
Descripción

Experimental drug, Dosage, Actual

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0237400
mg
Was cycle 1, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 1, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 2, day 1 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 2, day 1 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 2, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 2, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 3, day 1 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 3, day 1 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 3, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 3, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 4, day 1 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 4, day 1 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 4, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 4, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 5, day 1 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 5, day 1 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 5, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 5, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 6, day 1 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 6, day 1 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 6, day 8 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 6, day 8 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Investigational Product - IV Dosing (Carboplatin)
Descripción

Investigational Product - IV Dosing (Carboplatin)

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
Cycle Number
Descripción

Experimental drug, Dosage, chemotherapeutics regimen status cycle number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C2045829
Day
Descripción

Experimental drug, Dosage, Day

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0439228
Infusion Start Date
Descripción

Experimental drug, Dosage, Start Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0808070
Infusion Start Time
Descripción

Experimental drug, Dosage, Start Time

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1301880
Infusion Stop Date
Descripción

Experimental drug, Dosage, End Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0806020
Infusion Stop Time
Descripción

Experimental drug, Dosage, End Time

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1522314
Dose
Descripción

Experimental drug, Dosage

Tipo de datos

integer

Unidades de medida
  • AUC
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
AUC
Actual Dose
Descripción

Experimental drug, Dosage, Actual

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0237400
mg
Was cycle 2 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 2 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 3 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 3 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 4 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 4 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 5 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 5 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Was cycle 5 dose delayed?
Descripción

Experimental drug, Dosage, Delay of drug therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Delay of drug therapy, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1299700
UMLS CUI [1,4]
C0566251
Was cycle 5 dose reduced?
Descripción

Experimental drug, Dosage, Dose Reduced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
If Yes, check the Primary Reason
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Specify
Descripción

Experimental drug, Dosage, Dose Reduced, Reason and justification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1707814
UMLS CUI [1,4]
C0566251
Volver a la parte superior de la página

Similar models

Investigational Product - IV Dosing

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
Investigational Product - IV Dosing (Hycamtin)
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Item
Cycle Number
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2045829 (UMLS CUI [1,3])
Experimental drug, Dosing, Cycle, Numbers
Code List
Cycle Number
CL Item
1 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
2 (4)
CL Item
3 (5)
CL Item
3 (6)
CL Item
4 (7)
CL Item
4 (8)
CL Item
5 (9)
CL Item
5 (10)
CL Item
6 (11)
CL Item
6 (12)
Item
Day
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
Experimental drug, Dosing, Cycle, Numbers
Code List
Day
CL Item
1 (1)
CL Item
8 (2)
CL Item
1 (3)
CL Item
8 (4)
CL Item
1 (5)
CL Item
8 (6)
CL Item
1 (7)
CL Item
8 (8)
CL Item
1 (9)
CL Item
8 (10)
CL Item
1 (11)
CL Item
8 (12)
Experimental drug, Dosage, Start Date
Item
Infusion Start Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Time
Item
Infusion Start Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
Experimental drug, Dosage, End Date
Item
Infusion Stop Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Experimental drug, Dosage, End Time
Item
Infusion Stop Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
Experimental drug, Dosage
Item
Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Experimental drug, Dosage, Actual
Item
Actual Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0237400 (UMLS CUI [1,3])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 1, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 1, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 6, day 1 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 6, day 1 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 6, day 8 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 6, day 8 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Item Group
Investigational Product - IV Dosing (Carboplatin)
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Item
Cycle Number
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2045829 (UMLS CUI [1,3])
Experimental drug, Dosing, Cycle, Numbers
Code List
Cycle Number
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
Item
Day
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
Experimental drug, Dosing, Cycle, Numbers
Code List
Day
CL Item
1 (1)
CL Item
1 (2)
CL Item
1 (3)
CL Item
1 (4)
CL Item
1 (5)
CL Item
1 (6)
Experimental drug, Dosage, Start Date
Item
Infusion Start Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Experimental drug, Dosage, Start Time
Item
Infusion Start Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
Experimental drug, Dosage, End Date
Item
Infusion Stop Date
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Experimental drug, Dosage, End Time
Item
Infusion Stop Time
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
Experimental drug, Dosage
Item
Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Experimental drug, Dosage, Actual
Item
Actual Dose
integer
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0237400 (UMLS CUI [1,3])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 2 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 2 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 3 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 3 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 4 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 4 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy
Item
Was cycle 5 dose delayed?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1299700 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Delay of drug therapy, Reason and justification
Code List
Specify
Experimental drug, Dosage, Dose Reduced
Item
Was cycle 5 dose reduced?
boolean
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
Item
If Yes, check the Primary Reason
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Experimental drug, Dosage, Dose Reduced, Reason and justification
Code List
If Yes, check the Primary Reason
CL Item
Hematologic Toxicity (1)
CL Item
Non-Hematologic Toxicity (2)
CL Item
Other, specify (3)
Experimental drug, Dosage, Dose Reduced, Reason and justification
Item
Specify
text
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1707814 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial