ID

24748

Description

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

Mots-clés

  1. 16/08/2017 16/08/2017 -
  2. 16/08/2017 16/08/2017 -
  3. 16/08/2017 16/08/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

16 août 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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daily record card run-in period salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

daily record card run-in period salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Description

subject identifier

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Doctor’s name
Description

doctor's name

Type de données

text

Alias
UMLS CUI [1]
C2361125
Hospital/Clinic address
Description

hospital address

Type de données

text

Alias
UMLS CUI [1,1]
C0019994
UMLS CUI [1,2]
C1442065
Hospital/Clinic telephone number
Description

hospital telephone number

Type de données

integer

Alias
UMLS CUI [1]
C2986429
Next Clinic Visit
Description

Next Clinic Visit

Alias
UMLS CUI-1
C0008952
Date of next clinic visit
Description

date of next clinic visit

Type de données

date

Alias
UMLS CUI [1]
C2735342
Time of next clinic visit
Description

time of next clinic visit

Type de données

time

Alias
UMLS CUI [1,1]
C0008952
UMLS CUI [1,2]
C0040223

Similar models

daily record card run-in period salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
subject identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
doctor's name
Item
Doctor’s name
text
C2361125 (UMLS CUI [1])
hospital address
Item
Hospital/Clinic address
text
C0019994 (UMLS CUI [1,1])
C1442065 (UMLS CUI [1,2])
hospital telephone number
Item
Hospital/Clinic telephone number
integer
C2986429 (UMLS CUI [1])
Item Group
Next Clinic Visit
C0008952 (UMLS CUI-1)
date of next clinic visit
Item
Date of next clinic visit
date
C2735342 (UMLS CUI [1])
time of next clinic visit
Item
Time of next clinic visit
time
C0008952 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])

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