ID

38666

Descripción

Study ID: 106837 Clinical Study ID: HZA106837 Study Title: A Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects with Asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01086384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Relvar Study Indication: Asthma

Palabras clave

Versiones (4)
  1. 5/11/18 5/11/18 -
  2. 5/11/18 5/11/18 -
  3. 4/12/18 4/12/18 -
  4. 30/10/19 30/10/19 - Sarah Riepenhausen
Titular de derechos de autor

GSK group of companies

Subido en

30 de octubre 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 :

  • El más nuevo
  • Más antiguo
  • Popular
  • El más nuevo
    • El más nuevo
    • Más antiguo
    • Popular

Sin comentarios

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

A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Inglés

Concomitant Medications Form

1 formularios  
Concomitant Medication Details
Descripción

Concomitant Medication Details

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C1522508
Sequence Number
Descripción

Sequence Number

Tipo de datos

text

Alias
UMLS CUI [1]
C2348184
Drug Name
Descripción

Trade Name Preferred

Tipo de datos

text

Alias
UMLS CUI [1]
C2360065
Unit Dose
Descripción

Unit Dose

Tipo de datos

integer

Alias
UMLS CUI [1]
C0869039
Units
Descripción

Units

Tipo de datos

text

Alias
UMLS CUI [1]
C1519795
Medication Frequency
Descripción

Frequency

Tipo de datos

text

Alias
UMLS CUI [1]
C3476109
Medication Route
Descripción

Route

Tipo de datos

text

Alias
UMLS CUI [1]
C0013153
Reason for Medication
Descripción

Reason for Medication

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Generic dispensed?
Descripción

Generic dispensed?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3242750
UMLS CUI [1,2]
C0947323
Prescription or OTC?
Descripción

Prescription or OTC?

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0033080
UMLS CUI [2]
C0013231
Medication Start Date
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
Medication Taken prior to study?
Descripción

Taken prior to study?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C2603343
UMLS CUI [1,3]
C0332152
Medication Ongoing?
Descripción

Ongoing?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0549178
If NO, record the End Date
Descripción

If NO, record the End Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Device Used to Administer Medication
Descripción

Device Used to Administer Medication

Tipo de datos

text

Alias
UMLS CUI [1]
C0699733
UMLS CUI [2]
C0013227
Total Daily Dose
Descripción

Total Daily Dose

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2348070
UMLS CUI [1,2]
C0439810
Was drug administered for an exacerbation?
Descripción

Was drug administered for an exacerbation?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0806914
UMLS CUI [1,2]
C0349790
Was drug administered as a rescue medication?
Descripción

Was drug administered as a rescue medication?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0884980
Cumulative Dose Used?
Descripción

Cumulative Dose Used?

Tipo de datos

text

Alias
UMLS CUI [1]
C2986497
Was drug ever used?
Descripción

Was drug ever used?

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0242510
Drug usage Total duration
Descripción

Total duration

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0242510
UMLS CUI [1,2]
C0449238
Duration Unit
Descripción

Duration Unit

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C1519795
Medication Type
Descripción

Medication Type

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0332307
Volver a la parte superior de la página

Similar models

Concomitant Medications Form

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Concomitant Medication Details
C2347852 (UMLS CUI-1)
C1522508 (UMLS CUI-2)
Sequence Number
Item
Sequence Number
text
C2348184 (UMLS CUI [1])
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
Unit Dose
Item
Unit Dose
integer
C0869039 (UMLS CUI [1])
Units
Item
Units
text
C1519795 (UMLS CUI [1])
Frequency
Item
Medication Frequency
text
C3476109 (UMLS CUI [1])
Route
Item
Medication Route
text
C0013153 (UMLS CUI [1])
Reason for Medication
Item
Reason for Medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Generic dispensed?
Item
Generic dispensed?
boolean
C3242750 (UMLS CUI [1,1])
C0947323 (UMLS CUI [1,2])
Item
Prescription or OTC?
text
C0013227 (UMLS CUI [1,1])
C0033080 (UMLS CUI [1,2])
C0013231 (UMLS CUI [2])
Prescription of OTC?
Code List
Prescription or OTC?
CL Item
Prescription (1)
CL Item
OTC (2)
Start Date
Item
Medication Start Date
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Taken prior to study?
Item
Medication Taken prior to study?
boolean
C0013227 (UMLS CUI [1,1])
C2603343 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
Ongoing?
Item
Medication Ongoing?
boolean
C0013227 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
If NO, record the End Date
Item
If NO, record the End Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Device Used to Administer Medication
Item
Device Used to Administer Medication
text
C0699733 (UMLS CUI [1])
C0013227 (UMLS CUI [2])
Total Daily Dose
Item
Total Daily Dose
text
C2348070 (UMLS CUI [1,1])
C0439810 (UMLS CUI [1,2])
Was drug administered for an exacerbation?
Item
Was drug administered for an exacerbation?
boolean
C0806914 (UMLS CUI [1,1])
C0349790 (UMLS CUI [1,2])
Was drug administered as a rescue medication?
Item
Was drug administered as a rescue medication?
boolean
C0013227 (UMLS CUI [1,1])
C0884980 (UMLS CUI [1,2])
Cumulative Dose Used?
Item
Cumulative Dose Used?
text
C2986497 (UMLS CUI [1])
Was drug ever used?
Item
Was drug ever used?
boolean
C0242510 (UMLS CUI [1])
Total duration
Item
Drug usage Total duration
text
C0242510 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item
Duration Unit
text
C0449238 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Duration Unit
Code List
Duration Unit
CL Item
Days (1)
CL Item
Months (2)
CL Item
Weeks (3)
CL Item
Years (4)
Item
Medication Type
text
C0013227 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Medication Type
Code List
Medication Type
CL Item
Non-Asthma (1)
CL Item
Asthma (2)
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