ID
41465
Descripción
Study ID: 111114 Clinical Study ID: 111114 Study Title: A Randomized, Double-Blind, Parallel-Group, 24-Week Study to Evaluate the Efficacy and Safety of ADVAIR™ DISKUS™ (Fluticasone Propionate/Salmeterol Combination Product 250/50mcg Inhalation Powder) BID Plus Spiriva HandiHaler (Tiotropium Bromide Inhalation Powder 18mcg) QD Versus Spiriva QD Plus Placebo DISKUS BID in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00784550 https://clinicaltrials.gov/ct2/show/NCT00784550 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: N/A Trade Name: Tiotropium Bromide, Fluticasone Propionate/Salmeterol Study Indication: Pulmonary Disease, Chronic Obstructive The purpose of the study is to determine the efficacy and safety of the combination of ADVAIR DISKUS® 250/50mcg (FLUTICASONE PROPIONATE/SALMETEROL COMBINATION PRODUCT) plus SPIRIVA® HANDIHALER® inhaler 18mcg (TIOTROPIUM) compared to SPIRIVA® HANDIHALER® inhaler 18mcg (TIOTROPIUM) in patients with COPD. There are a total of 6 visits: Screening (Visit 1), Randomization (Visit 2), and after 4 (Visit 3), 8 (Visit 4), 16 (Visit 5) and 24 (Visit 6) weeks of treatment. This form (Demography) is to be filled out at the Screening (Visit 1).
Link
https://clinicaltrials.gov/ct2/show/NCT00784550
Palabras clave
Versiones (1)
- 20/10/20 20/10/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
20 de octubre de 2020
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 4.0
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Efficacy and Safety of ADVAIR DISKUS Plus Spiriva HandiHaler Versus Spiriva HandiHaler in COPD NCT00784550
Demography
- StudyEvent: ODM
Descripción
Demography
Alias
- UMLS CUI-1
- C0011298
Descripción
Date of birth
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0421451
Descripción
Sex
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0079399
Descripción
Ethnicity
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015031
Descripción
Geographic Ancestry: African American/African Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0085756
- UMLS CUI [3]
- C0027567
Descripción
Geographic Ancestry: American Indian or Alaskan Native
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1515945
Descripción
Geographic Ancestry: Asian - Central/South Asian Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238696
- UMLS CUI [3]
- C1519427
Descripción
Geographic Ancestry: Asian - East Asian Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C4540996
Descripción
Geographic Ancestry: Asian - Japanese Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1556094
Descripción
Geographic Ancestry: Asian - South East Asian Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238697
Descripción
Geographic Ancestry: Native Hawaiian or Other Pacific Islander
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1513907
Descripción
Geographic Ancestry: White - Arabic/North African Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238604
- UMLS CUI [3]
- C2698217
Descripción
Geographic Ancestry: White - White/Caucasian/European Heritage
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0043157
- UMLS CUI [3]
- C1535514
Similar models
Demography
- StudyEvent: ODM
C2985720 (UMLS CUI [2])
C0085756 (UMLS CUI [2])
C0027567 (UMLS CUI [3])
C1515945 (UMLS CUI [2])
C0238696 (UMLS CUI [2])
C1519427 (UMLS CUI [3])
C4540996 (UMLS CUI [2])
C1556094 (UMLS CUI [2])
C0238697 (UMLS CUI [2])
C1513907 (UMLS CUI [2])
C0238604 (UMLS CUI [2])
C2698217 (UMLS CUI [3])
C0043157 (UMLS CUI [2])
C1535514 (UMLS CUI [3])