ID
34978
Beschrijving
Study ID: 101888 Clinical Study ID: FFR101888 Study Title: A randomised, placebo-controlled, four way crossover study to evaluate the effect of double-blind 4000 mcg of orally inhaled GW685698X and of 6.25 mg cellobiose octa-acetate on electrocardiographic parameters, with single-blind 400 mg of oral moxifloxacin as a positive control, in 40 healthy male and female subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Veramyst,Avamys,Allermist Study Indication: Rhinitis, Allergic, Perennial The study consists of a screening, 4 treatment periods (TP) and a follow-up visit. For each TP there is a Day-1 (D-1) and a Day1 (D1). This document contains the Inhaler device training form. It has to be filled in for screening.
Trefwoorden
Versies (2)
- 04/02/2019 04/02/2019 -
- 06/02/2019 06/02/2019 - Sarah Riepenhausen
Houder van rechten
GlaxoSmithKline
Geüploaded op
6 de fevereiro de 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Effect of inhaled Fluticasone furoate and cellobiose octa-acetate on electrocardiographic parameters in healthy subjects, Study-ID: 101888
Inhaler device training
- StudyEvent: ODM
Beschrijving
Inhaler device training
Alias
- UMLS CUI-1
- C0030688
- UMLS CUI-2
- C0021461
Beschrijving
Use of Diskus
Datatype
text
Alias
- UMLS CUI [1,1]
- C1524063
- UMLS CUI [1,2]
- C0021461
- UMLS CUI [1,3]
- C1553480
- UMLS CUI [1,4]
- C0030688
Beschrijving
Note: If No, the subject is not eligible for the study.
Datatype
text
Alias
- UMLS CUI [1,1]
- C2349182
- UMLS CUI [1,2]
- C1524063
- UMLS CUI [1,3]
- C0021461
- UMLS CUI [1,4]
- C1553480
Similar models
Inhaler device training
- StudyEvent: ODM
C0021461 (UMLS CUI-2)
C0021461 (UMLS CUI [1,2])
C1553480 (UMLS CUI [1,3])
C0030688 (UMLS CUI [1,4])
C1524063 (UMLS CUI [1,2])
C0021461 (UMLS CUI [1,3])
C1553480 (UMLS CUI [1,4])
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