ID
33979
Descrizione
Study ID: 102936 Clinical Study ID: HZA102936 Study Title:A randomised, placebo-controlled, four-way crossover repeat dose study to evaluate the effect of the inhaled fluticasone furoate (FF)/GW642444M combination on electrocardiographic parameters, with moxifloxacin as a positive control, in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01209026 https://clinicaltrials.gov/ct2/show/NCT01209026?term=NCT01209026 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Allermist,Veramyst,Avamys; Veramyst,Avamys,Allermist Study Indication: Asthma The study consists of a screening, 4 treatment periods and a follow up. Treatment periods 1-4 are each 7 days long. Treatment period 1 Days 1-6 (TP1D-D6) Treatment period 1 Day 7 (TP1D7) Treatment period 2 Days 1-6 (TP2D1-D6) Treatment period 2 Day 7 (TP2D7) Treatment period 3 Days 1-6 (TP3D1-D6) Treatment period 3 Day 7 (TP3D7) Treatment period 4 Days 1-6 (TP4D1-D6) Treatment period 4 Day 7 (TP4D7) This document contains Electronically transferred laboratory data (Lab). It has to be filled in for screening, TP1-4 for each Day -1 and 7, follow-up and if required for Logs/Repeat.
collegamento
https://clinicaltrials.gov/ct2/show/NCT01209026?term=NCT01209026
Keywords
versioni (1)
- 09/01/19 09/01/19 -
Titolare del copyright
GlaxoSmithKline
Caricato su
9 gennaio 2019
DOI
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Licenza
Creative Commons BY-NC 3.0
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Effect of inhaled fluticasone furoate/Vilanterol combination on electrocardiographic parameters in healthy subjects, NCT01209026
Electronically transferred laboratory data (Lab)
- StudyEvent: ODM
Descrizione
Electronically transferred laboratory data (Lab) - Haematology
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0018941
Descrizione
If you tick 99 note date and time in following items.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C1277698
Descrizione
day month year
Tipo di dati
date
Alias
- UMLS CUI [1]
- C1302413
Descrizione
00:00-23:59. Time is optional. Use this item as the first item on this form. For additional tests, use the second item.
Tipo di dati
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0200345
Descrizione
Electronically transferred laboratory data (Lab) - Clinical chemistry
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
Descrizione
If you tick 99 note date and time in following items.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C1277698
Descrizione
day month year
Tipo di dati
date
Alias
- UMLS CUI [1]
- C1302413
Descrizione
00:00-23:59. Time is optional. Use this Item for all other samples on the form
Tipo di dati
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0200345
Descrizione
Electronically transferred laboratory data (Lab) - Urinalysis
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0042014
Descrizione
If you tick 99 note date and time in following items.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C1277698
Descrizione
day month year
Tipo di dati
date
Alias
- UMLS CUI [1]
- C1302413
Descrizione
00:00-23:59. Time is optional. Use this Item as the first Item on this form. For additional tests, use the second Item.
Tipo di dati
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0200345
Similar models
Electronically transferred laboratory data (Lab)
- StudyEvent: ODM
C0018941 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0008000 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0042014 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])