ID
32655
Beschreibung
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
Stichworte
Versionen (2)
- 09.11.18 09.11.18 -
- 09.11.18 09.11.18 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
9. November 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Fluticasone Furoate GW642444 Inhalation Powder and Fluticasone Furoate Inhalation Powder alone in the threatment of persistent asthma NCT01165138
Date of visit/ assessment, Subject Identification, Demography, Eligibility Question, Screen Failure, Investigator Signature, Previous Clinical Trial Participation - Screening
Beschreibung
Inform Enrollment
Alias
- UMLS CUI-1
- C1552002
- UMLS CUI-2
- C4041024
Beschreibung
Date of Visit/ Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-3
- C2985720
Beschreibung
Subject Identification
Alias
- UMLS CUI-1
- C1269815
Beschreibung
Demography
Alias
- UMLS CUI-1
- C0011298
Beschreibung
Date of birth
Datentyp
date
Alias
- UMLS CUI [1]
- C0421451
Beschreibung
Date of birth - Imputed
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0421451
- UMLS CUI [1,2]
- C2825504
Beschreibung
Sex
Datentyp
text
Alias
- UMLS CUI [1]
- C0079399
Beschreibung
Child- bearing potential
Datentyp
integer
Alias
- UMLS CUI [1]
- C3831118
Beschreibung
Date of final menses
Datentyp
date
Alias
- UMLS CUI [1]
- C0425932
Beschreibung
Date became sterile
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0021359
- UMLS CUI [1,2]
- C0011008
Beschreibung
Ethnicity
Datentyp
integer
Alias
- UMLS CUI [1]
- C0015031
Beschreibung
Geographic Ancestry
Datentyp
integer
Alias
- UMLS CUI [1]
- C3841890
Beschreibung
Subject Status
Datentyp
text
Alias
- UMLS CUI [1]
- C2348568
Beschreibung
Eligibility Question
Alias
- UMLS CUI-1
- C1516637
Beschreibung
If no, please select all the boxes corresponding to violations of any inclusion/ exclusion criteria
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C1512693
Beschreibung
If no, please select all the boxes corresponding to violations of any inclusion/ exclusion criteria
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C0680251
Beschreibung
Screen Failure
Alias
- UMLS CUI-1
- C1710476
Beschreibung
Screen failure
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1710476
Beschreibung
Screen failure date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0011008
Beschreibung
Reason for screen failure
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0566251
Beschreibung
If reason for screen failure is Investigator discretion, specify
Datentyp
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
Beschreibung
If reason for screen failure is withdrawn consent, specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [2,1]
- C1707492
- UMLS CUI [2,2]
- C2348235
Beschreibung
Investigator Siganture
Alias
- UMLS CUI-1
- C2346576
Beschreibung
Previous Clinical Trial Participation
Alias
- UMLS CUI-1
- C2348568
Beschreibung
Previous Fluticasone Furoate and/or GW642444 clinical trial
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C1948374
Beschreibung
Subject did participate in a previous Fluticasone Furoate and/or GW642444 clinical trial
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C1948374
Ähnliche Modelle
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])