ID

33999

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 the Dummy Dose form. It has to be filled in for TP1-4 for each D-1.

collegamento

https://clinicaltrials.gov/ct2/show/NCT01209026?term=NCT01209026

Keywords

  1. 09/01/19 09/01/19 -
  2. 10/01/19 10/01/19 - Sarah Riepenhausen
Titolare del copyright

GlaxoSmithKline

Caricato su

10 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Effect of inhaled fluticasone furoate/Vilanterol combination on electrocardiographic parameters in healthy subjects, NCT01209026

Dummy Dose

  1. StudyEvent: ODM
    1. Dummy Dose
Administrative data
Descrizione

Administrative data

Alias
UMLS CUI-1
C1320722
Subject number
Descrizione

Subject number

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Treatment period and Day
Descrizione

Treatment type/Treatment period and Day

Tipo di dati

integer

Alias
UMLS CUI [1]
C0087111
Dummy Dose
Descrizione

Dummy Dose

Alias
UMLS CUI-1
C3174092
UMLS CUI-2
C0304229
Date of Dummy dose
Descrizione

day month year

Tipo di dati

date

Alias
UMLS CUI [1,1]
C0032042
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
Time of Dummy dose
Descrizione

00:00-23:59

Tipo di dati

time

Alias
UMLS CUI [1,1]
C0032042
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0040223

Similar models

Dummy Dose

  1. StudyEvent: ODM
    1. Dummy Dose
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Item
Treatment period and Day
integer
C0087111 (UMLS CUI [1])
Code List
Treatment period and Day
CL Item
TP1D-1  (1)
(Comment:en)
CL Item
TP2D-1 (2)
(Comment:en)
CL Item
TP3D-1 (3)
(Comment:en)
CL Item
TP4D-1 (4)
(Comment:en)
Item Group
Dummy Dose
C3174092 (UMLS CUI-1)
C0304229 (UMLS CUI-2)
Date of Dummy dose
Item
Date of Dummy dose
date
C0032042 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Time of Dummy dose
Item
Time of Dummy dose
time
C0032042 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial