ID
34798
Description
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 status of treatment blind form, study conclusion, investigator's comment and signature. It has to be filled in for the end of study.
Keywords
Versions (3)
- 1/29/19 1/29/19 -
- 1/29/19 1/29/19 -
- 1/31/19 1/31/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
January 29, 2019
DOI
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License
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
Physical examination, medical condition
- StudyEvent: ODM
Description
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Description
Physical Examination, Systems
Data type
integer
Alias
- UMLS CUI [1]
- C0031809
Description
"Not done" only applicable for: Breasts, Urogenital, Pelvic and Rectal.
Data type
text
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C0449438
Description
Abnormal examination
Data type
text
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C0459424
Description
Medical condition
Alias
- UMLS CUI-1
- C0012634
Similar models
Physical examination, medical condition
- StudyEvent: ODM
C0459424 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,2])