ID
32656
Beschrijving
Study ID: 106827 Clinical Study ID: HZA106827 Study Title: HZA106827:A randomised, double-blind, placebo-controlled (with rescue medication), parallel group multicentre study of Fluticasone Furoate/GW642444 Inhalation Powder and Fluticasone Furoate Inhalation Powder alone in the treatment of persistent asthma in adults and adolescents Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01165138 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Allermist,Veramyst,Avamys; Relvar Study Indication: Asthma
Trefwoorden
Versies (2)
- 09-11-18 09-11-18 -
- 09-11-18 09-11-18 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
9 november 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Fluticasone Furoate GW642444 Inhalation Powder and Fluticasone Furoate Inhalation Powder alone in the treatment of persistent asthma NCT01165138
Date of visit/ assessment, Subject Identification, Demography, Eligibility Question, Screen Failure, Investigator Signature, Previous Clinical Trial Participation - Screening
Beschrijving
Inform Enrollment
Alias
- UMLS CUI-1
- C1552002
- UMLS CUI-2
- C4041024
Beschrijving
Date of Visit/ Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-3
- C2985720
Beschrijving
Subject Identification
Alias
- UMLS CUI-1
- C1269815
Beschrijving
Demography
Alias
- UMLS CUI-1
- C0011298
Beschrijving
Date of birth
Datatype
date
Alias
- UMLS CUI [1]
- C0421451
Beschrijving
Date of birth - Imputed
Datatype
date
Alias
- UMLS CUI [1,1]
- C0421451
- UMLS CUI [1,2]
- C2825504
Beschrijving
Sex
Datatype
text
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Child- bearing potential
Datatype
integer
Alias
- UMLS CUI [1]
- C3831118
Beschrijving
Date of final menses
Datatype
date
Alias
- UMLS CUI [1]
- C0425932
Beschrijving
Date became sterile
Datatype
date
Alias
- UMLS CUI [1,1]
- C0021359
- UMLS CUI [1,2]
- C0011008
Beschrijving
Ethnicity
Datatype
integer
Alias
- UMLS CUI [1]
- C0015031
Beschrijving
Geographic Ancestry
Datatype
integer
Alias
- UMLS CUI [1]
- C3841890
Beschrijving
Subject Status
Datatype
text
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
Eligibility Question
Alias
- UMLS CUI-1
- C1516637
Beschrijving
If no, please select all the boxes corresponding to violations of any inclusion/ exclusion criteria
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C1512693
Beschrijving
If no, please select all the boxes corresponding to violations of any inclusion/ exclusion criteria
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C0680251
Beschrijving
Screen Failure
Alias
- UMLS CUI-1
- C1710476
Beschrijving
Screen failure
Datatype
boolean
Alias
- UMLS CUI [1]
- C1710476
Beschrijving
Screen failure date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0011008
Beschrijving
Reason for screen failure
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0566251
Beschrijving
If reason for screen failure is Investigator discretion, specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [2,1]
- C0008961
- UMLS CUI [2,2]
- C0022423
- UMLS CUI [2,3]
- C2348235
Beschrijving
If reason for screen failure is withdrawn consent, specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [2,1]
- C1707492
- UMLS CUI [2,2]
- C2348235
Beschrijving
Investigator Siganture
Alias
- UMLS CUI-1
- C2346576
Beschrijving
Previous Clinical Trial Participation
Alias
- UMLS CUI-1
- C2348568
Beschrijving
Previous Fluticasone Furoate and/or GW642444 clinical trial
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C1948374
Beschrijving
Subject did participate in a previous Fluticasone Furoate and/or GW642444 clinical trial
Datatype
text
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C1948374
Similar models
Date of visit/ assessment, Subject Identification, Demography, Eligibility Question, Screen Failure, Investigator Signature, Previous Clinical Trial Participation - Screening
C2985720 (UMLS CUI-3)
C2985720 (UMLS CUI [1,2])
C2825504 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,2])
C0680251 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,2])
C0008961 (UMLS CUI [2,1])
C0022423 (UMLS CUI [2,2])
C2348235 (UMLS CUI [2,3])
C0566251 (UMLS CUI [1,2])
C1707492 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C1948374 (UMLS CUI [1,2])
C1948374 (UMLS CUI [1,2])