ID
26051
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 death
Keywords
Versions (6)
- 10/5/17 10/5/17 -
- 10/5/17 10/5/17 -
- 10/5/17 10/5/17 -
- 10/16/17 10/16/17 -
- 10/23/17 10/23/17 -
- 1/3/18 1/3/18 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 5, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Endpoint death GSK study Chronic Coronary Heart Disease NCT00799903
Endpoint death GSK study Chronic Coronary Heart Disease NCT00799903
Description
CEC Section
Description
[hidden]
Data type
integer
Description
cardiovascular death CHD
Data type
text
Description
Sudden death
Data type
integer
Description
other cardiovascular death - CHD specification
Data type
text
Description
death of unknown origin
Data type
integer
Description
cardiovascular death - Non-CHD
Data type
integer
Description
other vascular cause of death adjudication
Data type
text
Description
Specify in case of "other vascular cause of death" other than pulmonary embolism or peripheral arterial disease.
Data type
text
Description
non-cardiovascular death
Data type
text
Description
other non-cardiovascular death specification
Data type
text
Description
[hidden]
Data type
text
Description
[hidden]
Data type
date
Description
CEC Status
Description
[hidden]
Data type
text
Description
[read-only]
Data type
integer
Description
[read-only]
Data type
date
Description
[hidden]
Data type
integer
Description
[hidden]
Data type
date
Description
[hidden]
Data type
date
Description
[hidden]
Data type
integer
Description
[hidden]
Data type
date
Description
[hidden]
Data type
date
Description
[hidden]
Data type
text
Description
[hidden]
Data type
text
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
Description
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Data type
text