ID

24755

Descripción

Study ID: 100470 Clinical Study ID: SCO100470 Study Title: A multicentre, randomised, double-blind, parallel group, 24 week study to compare the effect of salmeterol/fluticasone propionate combination product 50/250mcg, with salmeterol 50mcg both delivered twice daily via DISKUS®/ACCUHALER® inhaler on lung function and dyspnoea in subjects with Chronic Obstructive Pulmonary Disease (COPD). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor:GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Serevent Study Indication: Pulmonary Disease, Chronic Obstructive

Palabras clave

  1. 16/8/17 16/8/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

16 de agosto de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Descripción

subject identifier

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
TRANSITION DYSPNOEA INDEX (TDI)
Descripción

TRANSITION DYSPNOEA INDEX (TDI)

Alias
UMLS CUI-1
C3714807
Date of assessment
Descripción

date of assessment

Tipo de datos

date

Alias
UMLS CUI [1]
C2985720
visit description
Descripción

visit description

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0678257
TDI Score
Descripción

transition dyspnoea index

Tipo de datos

integer

Alias
UMLS CUI [1]
C3714807

Similar models

transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
subject identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
TRANSITION DYSPNOEA INDEX (TDI)
C3714807 (UMLS CUI-1)
date of assessment
Item
Date of assessment
date
C2985720 (UMLS CUI [1])
Item
visit description
text
C0545082 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Code List
visit description
CL Item
Visit 3 (Visit 3)
CL Item
Visit 4 (Visit 4)
CL Item
Visit 5 (Visit 5)
CL Item
Visit 6 (Visit 6)
CL Item
Visit 7 (Visit 7)
CL Item
Visit 8 (Visit 8)
CL Item
Withdrawal (Withdrawal)
transition dyspnoea index
Item
TDI Score
integer
C3714807 (UMLS CUI [1])

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