ID

32502

Beschrijving

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

Trefwoorden

Versies (2)
  1. 05-11-18 05-11-18 -
  2. 04-12-18 04-12-18 -
Houder van rechten

GSK group of companies

Geüploaded op

5 november 2018

DOI

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Licentie

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

Engels

Pharmacogenetic Research Consent

1 Formulieren  
Pharmacogenetic (PGx) Research Consent/ Sample Collection
Beschrijving

Pharmacogenetic (PGx) Research Consent/ Sample Collection

Has informed consent been obtained for PGx reearch?
Beschrijving

Has informed consent been obtained for PGx reearch?

Datatype

boolean

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

if YES, record date informed consent obtained for PGx research

Datatype

text

If NO, check reason
Beschrijving

If NO, check reason

Datatype

text

If OTHER, specify
Beschrijving

If OTHER, specify

Datatype

text

Has sample been collected for PGx research?
Beschrijving

Has sample been collected for PGx research?

Datatype

boolean

If YES, record the date sample taken
Beschrijving

If YES, record the date sample taken

Datatype

date

Sample Type
Beschrijving

Sample Type

Record Sample Type
Beschrijving

Record Sample Type

Datatype

text

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Similar models

Pharmacogenetic Research Consent

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Terug naar het begin van de pagina 

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