ID
33414
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 (2)
- 7/11/18 7/11/18 -
- 7/12/18 7/12/18 -
Titular de derechos de autor
GSK group of companies
Subido en
7 de diciembre de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837
Patient's Diary Card 1: Screening/Run-In Visit 1
- StudyEvent: ODM
Descripción
Daily Assessments
Alias
- UMLS CUI-1
- C0220825
- UMLS CUI-2
- C0332173
Descripción
Date
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2985720
Descripción
0 = No symptoms during the day or previous night 1 = Symptoms for one short period during the day or previous night 2 = Symptoms for two or more short periods during the day or previous night 3 = Symptoms for most of the day or previous night which did not affect my normal activities 4 = Symptoms for most of the day or previous night which did affect my normal activities 5 = Symptoms so severe that I could not go to work or perform normal activities Circle only one number
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0004096
- UMLS CUI [1,2]
- C1457887
Descripción
if nono, enter zero (0)
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1533107
- UMLS CUI [1,2]
- C0001927
Similar models
Patient's Diary Card 1: Screening/Run-In Visit 1
- StudyEvent: ODM
C1457887 (UMLS CUI [1,2])
C0001927 (UMLS CUI [1,2])
Sin comentarios