ID
34880
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 vital signs form. It has to be filled in for screening.
Mots-clés
Versions (2)
- 31/01/2019 31/01/2019 -
- 01/02/2019 01/02/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
1 février 2019
DOI
Pour une demande vous connecter.
Licence
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
Vital signs for screening
- StudyEvent: ODM
Description
Vital Signs
Alias
- UMLS CUI-1
- C0518766
Description
Body height
Type de données
integer
Unités de mesure
- cm
Alias
- UMLS CUI [1]
- C0005890
Description
Note: if the Body Weight is < 50 kg, the subject is not eligible for the study.
Type de données
float
Unités de mesure
- kg
Alias
- UMLS CUI [1]
- C0005910
Description
Provide the body mass index calculated using the following formula: Body Mass index = (Weight (kg) / (Height (cm))²) x 10.000 Note: if the Body Mass Index is not within range of 19-31 kg/cm2 inclusive, the subject is not eligible for the study.
Type de données
float
Unités de mesure
- kg/m2
Alias
- UMLS CUI [1]
- C1305855
Description
day month year
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0518766
Description
Three measurements, at least 2 minutes apart, will be taken at each specified time -the subject having rested in the supine position for at least 5 minutes before the first measurement. At screening only, the supine measurements will be followed by measurements in the erect position immediately after standing.
Type de données
integer
Alias
- UMLS CUI [1]
- C0439564
Description
00:00-23:59
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0518766
Description
Ensure that blood pressure values are within reasonable limits and systolic blood pressure is greater than diastolic blood pressure.
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Ensure that blood pressure values are within reasonable limits and systolic blood pressure is greater than diastolic blood pressure.
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Subject position
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1262869
- UMLS CUI [1,2]
- C0518766
Description
Ensure that heart rate value is within reasonable limits for beats per minute.
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1,1]
- C0018810
- UMLS CUI [1,2]
- C0518766
Similar models
Vital signs for screening
- StudyEvent: ODM
C0518766 (UMLS CUI [1,2])
C0518766 (UMLS CUI [1,2])
C0518766 (UMLS CUI [1,2])