ID

33406

Description

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

Keywords

Versions (2)
  1. 11/6/18 11/6/18 -
  2. 12/7/18 12/7/18 -
Copyright Holder

GSK group of companies

Uploaded on

December 7, 2018

DOI

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License

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

English

Pharmacokinetics (Liver PK)

1 forms  
An unscheduled PK sample must be obtained within 24 hours of last dose
Description

An unscheduled PK sample must be obtained within 24 hours of last dose

Alias
UMLS CUI-1
C0201734
UMLS CUI-2
C0370003
Was a pharmacokinetic blood sample obtained?
Description

Was a pharmacokinetic blood sample obtained?

Data type

boolean

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
If YES, record date sample taken
Description

If YES, record date sample taken

Data type

date

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0011008
If YES, record time sample taken
Description

If YES, record time sample taken

Data type

time

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0040223
Date of last investigational product dose prior to PK sample
Description

Date of last investigational product dose prior to PK sample

Data type

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C1762893
UMLS CUI [2,1]
C0201734
UMLS CUI [2,2]
C0370003
Time of last investigational product dose prior to PK sample
Description

Time of last investigational product dose prior to PK sample

Data type

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0946444
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Similar models

Pharmacokinetics (Liver PK)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
An unscheduled PK sample must be obtained within 24 hours of last dose
C0201734 (UMLS CUI-1)
C0370003 (UMLS CUI-2)
Was a pharmacokinetic blood sample obtained?
Item
Was a pharmacokinetic blood sample obtained?
boolean
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
If YES, record date sample taken
Item
If YES, record date sample taken
date
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
If YES, record time sample taken
Item
If YES, record time sample taken
time
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Date of last investigational product dose prior to PK sample
Item
Date of last investigational product dose prior to PK sample
date
C0304229 (UMLS CUI [1,1])
C1762893 (UMLS CUI [1,2])
C0201734 (UMLS CUI [2,1])
C0370003 (UMLS CUI [2,2])
Time of last investigational product dose prior to PK sample
Item
Time of last investigational product dose prior to PK sample
time
C0304229 (UMLS CUI [1,1])
C0946444 (UMLS CUI [1,2])
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