ID
28314
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
January 3, 2018
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
Alias
- UMLS CUI [1]
- C3260278
Description
cardiovascular death CHD
Data type
text
Alias
- UMLS CUI [1]
- C0010068
Description
Sudden death
Data type
integer
Alias
- UMLS CUI [1]
- C0011071
Description
other cardiovascular death - CHD specification
Data type
text
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C2348235
Description
death of unknown origin
Data type
integer
Alias
- UMLS CUI [1]
- C0277589
Description
cardiovascular death - Non-CHD
Data type
integer
Alias
- UMLS CUI [1]
- C0010068
Description
other vascular cause of death adjudication
Data type
text
Alias
- UMLS CUI [1]
- C0007465
Description
Specify in case of "other vascular cause of death" other than pulmonary embolism or peripheral arterial disease.
Data type
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0007465
Description
non-cardiovascular death
Data type
text
Alias
- UMLS CUI [1]
- C0007465
Description
other non-cardiovascular death specification
Data type
text
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C2348235
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C1536080
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1]
- C3260278
Description
CEC Status
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C2736071
Description
[read-only]
Data type
integer
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]
- C2826892
Description
[hidden]
Data type
date
Alias
- UMLS CUI [1,1]
- C1515023
- UMLS CUI [1,2]
- C0011008
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
Alias
- UMLS CUI [1]
- C0947611
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
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
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