ID
44432
Description
Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Endpoint Hospitalisation for heart failure - Repeating form (Scheduled visits)
Keywords
Versions (6)
- 10/7/17 10/7/17 -
- 10/16/17 10/16/17 -
- 10/23/17 10/23/17 -
- 1/11/18 1/11/18 -
- 1/14/18 1/14/18 -
- 9/20/21 9/20/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
September 20, 2021
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Endpoint Hospitalisation for heart failure GSK study Chronic Coronary Heart Disease NCT00799903
Endpoint Hospitalisation for heart failure GSK study Chronic Coronary Heart Disease NCT00799903
Description
CEC Section
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C0680730
Description
criteria for heart failure not met specification
Data type
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0018801
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1]
- C3260278
Description
CEC Status
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C1444748
Description
[read-only]
Data type
integer
Alias
- UMLS CUI [1]
- C0449438
Description
[read-only]
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0443172
Description
[hidden]
Data type
integer
Alias
- UMLS CUI [1]
- C0184806
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Data type
integer
Alias
- UMLS CUI [1]
- C0184806
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C2826275
Description
Use SAE Sequence number from the corresponding SAE form (the last item on the form, in the "Non-Clinical" section) [hidden].
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348585
Description
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Data type
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
Similar models
Endpoint Hospitalisation for heart failure GSK study Chronic Coronary Heart Disease NCT00799903
C1320528 (UMLS CUI [1,2])
C0012798 (UMLS CUI [1,2])
C0012798 (UMLS CUI [1,2])
C1522609 (UMLS CUI [1,2])
C1095989 (UMLS CUI [1,2])
C0669479 (UMLS CUI [1,2])
C0686905 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C0686905 (UMLS CUI [1,3])
C0669479 (UMLS CUI [1,2])
C0686905 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0018801 (UMLS CUI [1,2])
C0443172 (UMLS CUI [1,2])
C3166277 (UMLS CUI [1,2])
C1515023 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C3166277 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C3166277 (UMLS CUI [1,2])
C1515023 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C3166277 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C2348585 (UMLS CUI [1,2])
C2826934 (UMLS CUI [1,2])