ID
34978
Beskrivning
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.
Nyckelord
Versioner (2)
- 2019-02-04 2019-02-04 -
- 2019-02-06 2019-02-06 - Sarah Riepenhausen
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
6 februari 2019
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Effect of inhaled Fluticasone furoate and cellobiose octa-acetate on electrocardiographic parameters in healthy subjects, Study-ID: 101888
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])
Inga kommentarer