ID

37140

Description

Study ID: 104864/502 Clinical Study ID: 104864/502 Study Title: An Open-Label, Multicenter, Randomized, Phase II Study of Oral Topotecan Daily x 5 Days vs. Oral Topotecan 5 Days On, 2 Days Off for 3 Weeks for Second-Line Treatment in Patients with Recurrent, Locally Advanced or Metastatic Cervical Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan Trade Name: N/A Study Indication: Cancer, Locally Advanced or Metastatic Cervical Cancer

Mots-clés

Versions (1)
  1. 4/7/19 4/7/19 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

4 de julio de 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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Oral Topotecan Daily x 5 Days vs. Oral Topotacan 5 Days On, 2 Days Off; 104864/502

Anglais

Laboratory Reference Ranges

1 Formulaires  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Center Number
Description

Institution name, Identifier

Type de données

integer

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0600091
Laboratory Reference Ranges
Description

Laboratory Reference Ranges

Alias
UMLS CUI-1
C0883335
Investigator
Description

Reference lab test reference range, Investigator Name

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C2826892
Lab Number Code
Description

Reference lab test reference range, Laboratory, Code

Type de données

integer

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0022877
UMLS CUI [1,3]
C0805701
Laboratory Name
Description

Reference lab test reference range, Performing laboratory name

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C3258037
Address
Description

Reference lab test reference range, Performing laboratory name, Address

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C3258037
UMLS CUI [1,3]
C1442065
Mark One
Description

Reference lab test reference range, Gender

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0079399
Date on which these reference ranges became effective
Description

Reference lab test reference range, Start Date

Type de données

date

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0808070
Age Range
Description

Reference lab test reference range, Age, Range

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0001779
UMLS CUI [1,3]
C1514721
Test
Description

Reference lab test reference range, Laboratory Procedures

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0022885
Unit
Description

Reference lab test reference range, Unit

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0439148
Low Reference Value
Description

Reference lab test reference range, Lower Limit of Reference Range

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C1272773
High Reference Value
Description

Reference lab test reference range, Upper Limit of Reference Range

Type de données

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C1299400
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Similar models

Laboratory Reference Ranges

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Institution name, Identifier
Item
Center Number
integer
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Item Group
Laboratory Reference Ranges
C0883335 (UMLS CUI-1)
Reference lab test reference range, Investigator Name
Item
Investigator
text
C0883335 (UMLS CUI [1,1])
C2826892 (UMLS CUI [1,2])
Reference lab test reference range, Laboratory, Code
Item
Lab Number Code
integer
C0883335 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Reference lab test reference range, Performing laboratory name
Item
Laboratory Name
text
C0883335 (UMLS CUI [1,1])
C3258037 (UMLS CUI [1,2])
Reference lab test reference range, Performing laboratory name, Address
Item
Address
text
C0883335 (UMLS CUI [1,1])
C3258037 (UMLS CUI [1,2])
C1442065 (UMLS CUI [1,3])
Item
Mark One
text
C0883335 (UMLS CUI [1,1])
C0079399 (UMLS CUI [1,2])
Reference lab test reference range, Gender
Code List
Mark One
CL Item
Male Reference Range  (1)
CL Item
Female Reference Range (2)
Reference lab test reference range, Start Date
Item
Date on which these reference ranges became effective
date
C0883335 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Reference lab test reference range, Age, Range
Item
Age Range
text
C0883335 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
C1514721 (UMLS CUI [1,3])
Item
Test
text
C0883335 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
Reference lab test reference range, Laboratory Procedures
Code List
Test
CL Item
Hemoglobin (1)
CL Item
Hematocrit (2)
CL Item
RBC (3)
CL Item
WBC (4)
CL Item
Neutrophils-segmented (5)
CL Item
Bands (6)
CL Item
Lymphocytes (7)
CL Item
Monocytes (8)
CL Item
Eosinophils (9)
CL Item
Basophils (10)
CL Item
Platelets (11)
Reference lab test reference range, Unit
Item
Unit
text
C0883335 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
Reference lab test reference range, Lower Limit of Reference Range
Item
Low Reference Value
text
C0883335 (UMLS CUI [1,1])
C1272773 (UMLS CUI [1,2])
Reference lab test reference range, Upper Limit of Reference Range
Item
High Reference Value
text
C0883335 (UMLS CUI [1,1])
C1299400 (UMLS CUI [1,2])
Retour au début de la page 

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