ID
34977
Descripción
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 standard meal form. It has to be filled in for TP1-4 Day1.
Palabras clave
Versiones (2)
- 4/2/19 4/2/19 -
- 6/2/19 6/2/19 - Sarah Riepenhausen
Titular de derechos de autor
GlaxoSmithKline
Subido en
6 de febrero de 2019
DOI
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Licencia
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
Standard meal
- StudyEvent: ODM
Descripción
Standard meal
Alias
- UMLS CUI-1
- C0444664
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0444664
Descripción
Time Relative To Dosing
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0444664
Descripción
00:00-23:59
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0444664
Descripción
Ingestion of meal
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1998602
- UMLS CUI [1,2]
- C0205197
Similar models
Standard meal
- StudyEvent: ODM
C0444664 (UMLS CUI [1,2])
C0444664 (UMLS CUI [1,2])
C0444664 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,2])