ID
34846
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 PGx-Pharmacogenetic research form. It has to be filled in for the end of study.
Palabras clave
Versiones (2)
- 2019-01-31 2019-01-31 -
- 2019-02-01 2019-02-01 - Sarah Riepenhausen
Titular de derechos de autor
GlaxoSmithKline
Subido en
31 januari 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
PGx-Pharmacogenetic research
- StudyEvent: ODM
Descripción
PGx-Pharmacogenetic research consent
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C2347500
Descripción
Consent for PGx-Pharmacogenetic research
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2347500
Descripción
tick one reason
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2347500
- UMLS CUI [2]
- C0566251
Descripción
Other reason for non consent for PGx-Pharmacogenetic research
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2347500
- UMLS CUI [2,1]
- C0205394
- UMLS CUI [2,2]
- C0566251
Descripción
Blood sample collection (DNA)
Alias
- UMLS CUI-1
- C0005834
- UMLS CUI-2
- C2347500
Descripción
Blood sample collected for PGx-pharmacogenetic research
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C2347500
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C2347500
Descripción
Withdrawl of consent
Alias
- UMLS CUI-1
- C1707492
Descripción
This question must be completed immediately if the subject withdraws consent. Otherwise, it must be completed when the subject leaves the study. It must be completed for all subjects for whom informed consent was obtained for PGx-Pharmacogenetic research.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C1707492
Descripción
Blood sample destruction
Alias
- UMLS CUI-1
- C1948029
- UMLS CUI-2
- C0178913
Descripción
This question must be completed immediately if there is a request for sample destruction. Otherwise, it must be completed when the subject leaves the study. It must be completed for all subjects for whom a blood sample was obtained for PGx-Pharmacogenetic research.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1272683
- UMLS CUI [1,2]
- C1948029
- UMLS CUI [1,3]
- C0178913
Descripción
Tick one reason
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1272683
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C0178913
Descripción
Other reason for request for sample destruction
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C1948029
- UMLS CUI [1,5]
- C0178913
Similar models
PGx-Pharmacogenetic research
- StudyEvent: ODM
C2347500 (UMLS CUI-2)
C2347500 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,3])
C0566251 (UMLS CUI [2])
C0021430 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,3])
C0205394 (UMLS CUI [2,1])
C0566251 (UMLS CUI [2,2])
C2347500 (UMLS CUI-2)
C2347500 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,3])
C1707492 (UMLS CUI [1,2])
C0178913 (UMLS CUI-2)
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C1948029 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,5])