ID

32502

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 (2)
  1. 5/11/18 5/11/18 -
  2. 4/12/18 4/12/18 -
Titular de derechos de autor

GSK group of companies

Subido en

5 de noviembre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Inglés

Pharmacogenetic Research Consent

1 formularios  
Pharmacogenetic (PGx) Research Consent/ Sample Collection
Descripción

Pharmacogenetic (PGx) Research Consent/ Sample Collection

Has informed consent been obtained for PGx reearch?
Descripción

Has informed consent been obtained for PGx reearch?

Tipo de datos

boolean

if YES, record date informed consent obtained for PGx research
Descripción

if YES, record date informed consent obtained for PGx research

Tipo de datos

text

If NO, check reason
Descripción

If NO, check reason

Tipo de datos

text

If OTHER, specify
Descripción

If OTHER, specify

Tipo de datos

text

Has sample been collected for PGx research?
Descripción

Has sample been collected for PGx research?

Tipo de datos

boolean

If YES, record the date sample taken
Descripción

If YES, record the date sample taken

Tipo de datos

date

Sample Type
Descripción

Sample Type

Record Sample Type
Descripción

Record Sample Type

Tipo de datos

text

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Similar models

Pharmacogenetic Research Consent

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Pharmacogenetic (PGx) Research Consent/ Sample Collection
Has informed consent been obtained for PGx reearch?
Item
Has informed consent been obtained for PGx reearch?
boolean
if YES, record date informed consent obtained for PGx research
Item
if YES, record date informed consent obtained for PGx research
text
Item
If NO, check reason
text
If NO, check reason
Code List
If NO, check reason
CL Item
[1] Subject declined (1)
CL Item
[2] Subject not asked by Investigator (2)
CL Item
[Z] Other (3)
If OTHER, specify
Item
If OTHER, specify
text
Has sample been collected for PGx research?
Item
Has sample been collected for PGx research?
boolean
If YES, record the date sample taken
Item
If YES, record the date sample taken
date
Item Group
Sample Type
Record Sample Type
Item
Record Sample Type
text
Volver a la parte superior de la página 

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