ID

24753

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

Keywords

Versions (3)
  1. 8/16/17 8/16/17 -
  2. 8/16/17 8/16/17 -
  3. 8/16/17 8/16/17 -
Uploaded on

August 16, 2017

DOI

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License

Creative Commons BY-NC 3.0
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daily record card administration salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

English

daily record card administration salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

1 forms  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
time of documentation
Description

time of documentation

Data type

text

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0920316
Subject Identifier
Description

subject identifier

Data type

integer

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

doctor's name

Data type

text

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

hospital address

Data type

text

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

hospital telephone number

Data type

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

Data type

date

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

time of next clinic visit

Data type

time

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

daily record card administration salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Item
time of documentation
text
C0040223 (UMLS CUI [1,1])
C0920316 (UMLS CUI [1,2])
time of assessment
Code List
time of documentation
CL Item
run-in period (RUN-IN PERIOD)
CL Item
treatment period visit 2 (TREATMENT PERIOD Visit 2)
CL Item
treatment period visit 3 (TREATMENT PERIOD Visit 3)
CL Item
treatment period visit 4 (TREATMENT PERIOD Visit 4)
CL Item
treatment period visit 5 (TREATMENT PERIOD Visit 5)
CL Item
treatment period visit 6 (TREATMENT PERIOD Visit 6)
CL Item
treatment period visit 7 (TREATMENT PERIOD Visit 7)
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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