ID

29528

Beschrijving

Study ID: 102871 Clinical Study ID: HZC102871 Study Title:HZC102871: A 52-week efficacy and safety study to compare the effect of three dosage strengths of Fluticasone Furoate/GW642444 Inhalation Powder with GW642444 on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01009463 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Veramyst,Avamys,Allermist Study Indication: Pulmonary Disease, Chronic Obstructive Documentation part: Pharmacogenetic Research Consent / Sample Collection

Trefwoorden

Versies (2)
  1. 04-03-18 04-03-18 -
  2. 05-04-18 05-04-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

5 april 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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GSK Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) NCT01009463

Engels

Pharmacogenetic Research Consent / Sample Collection

1 Formulieren  
Pharmacogenetic Research Consent / Sample Collection
Beschrijving

Pharmacogenetic Research Consent / Sample Collection

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C0021430
UMLS CUI-3
C2347500
Has informed consent been obtained for PGx research?
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Date informed consent obtained for Px research
Beschrijving

Date informed consent obtained

Datatype

date

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0011008
Has sample been collected for PGx research?
Beschrijving

sample collection

Datatype

boolean

Alias
UMLS CUI [1]
C0005834
Yes, record date sample taken
Beschrijving

sample collection date

Datatype

date

Alias
UMLS CUI [1]
C1302413
No, check reason sample not collected
Beschrijving

reason sample not collected

Datatype

integer

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0392360
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Similar models

Pharmacogenetic Research Consent / Sample Collection

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Pharmacogenetic Research Consent / Sample Collection
C0008976 (UMLS CUI-1)
C0021430 (UMLS CUI-2)
C2347500 (UMLS CUI-3)
informed consent
Item
Has informed consent been obtained for PGx research?
boolean
C0021430 (UMLS CUI [1])
Date informed consent obtained
Item
Date informed consent obtained for Px research
date
C0021430 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
sample collection
Item
Has sample been collected for PGx research?
boolean
C0005834 (UMLS CUI [1])
sample collection date
Item
Yes, record date sample taken
date
C1302413 (UMLS CUI [1])
Item
No, check reason sample not collected
integer
C0200345 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
reason sample not collected
Code List
No, check reason sample not collected
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other, specify (3)
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