ID
40701
Descripción
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
Palabras clave
Versiones (3)
- 30/10/18 30/10/18 -
- 26/11/18 26/11/18 -
- 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor
GSK group of companies
Subido en
30 de abril de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837
Administrative and Demography Form
- StudyEvent: ODM
Descripción
Inform Enrollment
Alias
- UMLS CUI-1
- C1552002
- UMLS CUI-2
- C4041024
Descripción
Date of Visit/ Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Descripción
Subject Identification
Alias
- UMLS CUI-1
- C2348585
Descripción
Demography Data
Alias
- UMLS CUI-1
- C0011298
Descripción
Or age in years
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0421451
Descripción
Age should be completed for subjects at German sites only. For all other subjects complete Date of Birth.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0001779
Descripción
Sex
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0079399
Descripción
Ethnicity
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015031
Descripción
check all that apply
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3841890
Descripción
Subject Status
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0681850
- UMLS CUI [1,2]
- C0449438
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