ID
33699
Description
Study ID: 102936 Clinical Study ID: HZA102936 Study Title:A randomised, placebo-controlled, four-way crossover repeat dose study to evaluate the effect of the inhaled fluticasone furoate (FF)/GW642444M combination on electrocardiographic parameters, with moxifloxacin as a positive control, in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01209026 https://clinicaltrials.gov/ct2/show/NCT01209026?term=NCT01209026 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Allermist,Veramyst,Avamys; Veramyst,Avamys,Allermist Study Indication: Asthma The study consists of a screening, 8 treatment periods and a follow up. Treatment periods 1-4 are each 7 days long. Treatment period 1 Days 1-6 (TP1D-D6) Treatment period 1 Day 7 (TP1D7) Treatment period 2 Days 1-6 (TP2D1-D6) Treatment period 2 Day 7 (TP2D7) Treatment period 3 Days 1-6 (TP3D1-D6) Treatment period 3 Day 7 (TP3D7) Treatment period 4 Days 1-6 (TP4D1-D6) Treatment period 4 Day 7 (TP4D7) This document contains the Demography of subject and subject data. It has to be filled in for screening.
Lien
https://clinicaltrials.gov/ct2/show/NCT01209026?term=NCT01209026
Mots-clés
Versions (2)
- 19.12.18 19.12.18 -
- 20.12.18 20.12.18 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
20. Dezember 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
Modèle Commentaires :
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Effect of inhaled fluticasone furoate/Vilanterol combination on electrocardiographic parameters in healthy subjects, NCT01209026
Demography, subject data
- StudyEvent: ODM
Description
Subject data
Alias
- UMLS CUI-1
- C1997894
- UMLS CUI-2
- C2986440
Description
Item is not required
Type de données
text
Alias
- UMLS CUI [1,1]
- C1997894
- UMLS CUI [1,2]
- C2986440
Description
day month year
Type de données
date
Alias
- UMLS CUI [1]
- C0421451
Description
Sex
Type de données
text
Alias
- UMLS CUI [1]
- C0079399
Description
Child-bearing potential
Type de données
integer
Alias
- UMLS CUI [1]
- C3831118
Description
Ethnicity
Alias
- UMLS CUI-1
- C0015031
Description
Geographic Ancestry
Alias
- UMLS CUI-1
- C0034510
Description
African American/African Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C0085756
- UMLS CUI [2]
- C0027567
Description
American Indian or Alaskan Native
Type de données
boolean
Alias
- UMLS CUI [1]
- C1515945
Description
Asian - central/South Asian Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C0238696
- UMLS CUI [2]
- C1519427
Description
Asian - East Asian Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C4540996
Description
Asian - Japanese Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C1556094
Description
Asian - South East Asian Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C0238697
Description
Native Hawaiian or Other Pacific Islander
Type de données
boolean
Alias
- UMLS CUI [1]
- C1513907
Description
White - Arabic/North African Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C0238604
- UMLS CUI [2]
- C0026068
Description
White - White/Caucasian/European Heritage
Type de données
boolean
Alias
- UMLS CUI [1]
- C0043157
Similar models
Demography, subject data
- StudyEvent: ODM
C2986440 (UMLS CUI [1,2])
C0027567 (UMLS CUI [2])
C1519427 (UMLS CUI [2])
C0026068 (UMLS CUI [2])