ID
34939
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 Serology - screen for HIV antibody, hepatitis B and C form. It has to be filled in for screening.
Keywords
Versions (1)
- 2/4/19 2/4/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
February 4, 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
Serology - screen for HIV antibody, hepatitis B and C
- StudyEvent: ODM
Description
Serology - screen for HIV antibody, hepatitis B and C
Alias
- UMLS CUI-1
- C0036743
- UMLS CUI-2
- C0019682
- UMLS CUI-3
- C0019163
- UMLS CUI-4
- C0019196
Description
day month year
Data type
date
Alias
- UMLS CUI [1]
- C1302413
Description
Tick for each test a result
Data type
integer
Alias
- UMLS CUI [1]
- C0036743
Description
Tick appropriate box(es). Note: If any of the tests are positive, the subject is not eligible for the study.
Data type
text
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0036743
Similar models
Serology - screen for HIV antibody, hepatitis B and C
- StudyEvent: ODM
C0019682 (UMLS CUI-2)
C0019163 (UMLS CUI-3)
C0019196 (UMLS CUI-4)
C0036743 (UMLS CUI [1,2])