ID

32502

Descrição

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

Palavras-chave

Versões (2)
  1. 05/11/2018 05/11/2018 -
  2. 04/12/2018 04/12/2018 -
Titular dos direitos

GSK group of companies

Transferido a

5 de novembro de 2018

DOI

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Licença

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

Inglês

Pharmacogenetic Research Consent

1 Formulários  
Pharmacogenetic (PGx) Research Consent/ Sample Collection
Descrição

Pharmacogenetic (PGx) Research Consent/ Sample Collection

Has informed consent been obtained for PGx reearch?
Descrição

Has informed consent been obtained for PGx reearch?

Tipo de dados

boolean

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

if YES, record date informed consent obtained for PGx research

Tipo de dados

text

If NO, check reason
Descrição

If NO, check reason

Tipo de dados

text

If OTHER, specify
Descrição

If OTHER, specify

Tipo de dados

text

Has sample been collected for PGx research?
Descrição

Has sample been collected for PGx research?

Tipo de dados

boolean

If YES, record the date sample taken
Descrição

If YES, record the date sample taken

Tipo de dados

date

Sample Type
Descrição

Sample Type

Record Sample Type
Descrição

Record Sample Type

Tipo de dados

text

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Similar models

Pharmacogenetic Research Consent

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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
Voltar ao início da página 

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