ID
28375
Beschrijving
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 unstable angina - Repeating form (Scheduled visits)
Trefwoorden
Versies (4)
- 07-10-17 07-10-17 -
- 16-10-17 16-10-17 -
- 23-10-17 23-10-17 -
- 09-01-18 09-01-18 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
9 januari 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Endpoint Hospitalisation for unstable angina GSK study Chronic Coronary Heart Disease NCT00799903
Endpoint Hospitalisation for unstable angina GSK study Chronic Coronary Heart Disease NCT00799903
Beschrijving
CEC Section
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C3260278
Beschrijving
Adjudication Ischemic discomfort at rest
Datatype
text
Alias
- UMLS CUI [1,1]
- C0008031
- UMLS CUI [1,2]
- C0035253
Beschrijving
adjudication ischemic discomfort at rest duration
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0235710
- UMLS CUI [1,2]
- C0035253
- UMLS CUI [1,3]
- C3260278
Beschrijving
criteria for unstable angina not met specification
Datatype
text
Alias
- UMLS CUI [1]
- C0002965
Beschrijving
criteria for MI met
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3897171
- UMLS CUI [1,2]
- C0027051
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C1536080
Beschrijving
Only to be completed for events adjudicated to be an MI [hidden]
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0027051
- UMLS CUI [1,2]
- C0680730
Beschrijving
Only to be completed for events adjudicated to be an MI [hidden]
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0027051
- UMLS CUI [1,2]
- C0008902
Beschrijving
MI adjudication acute
Datatype
text
Alias
- UMLS CUI [1]
- C0155626
Beschrijving
MI adjudication prior
Datatype
text
Alias
- UMLS CUI [1]
- C1275835
Beschrijving
Only to be completed for events adjudicated to be an MI [hidden]
Datatype
text
Alias
- UMLS CUI [1,1]
- C1536220
- UMLS CUI [1,2]
- C3537184
Beschrijving
Only to be completed for events adjudicated to be an MI [hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C1305738
Beschrijving
Only to be completed for events adjudicated to be an MI [hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C0027051
Beschrijving
[hidden]
Datatype
date
Alias
- UMLS CUI [1]
- C3260278
Beschrijving
CEC Status
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C1444748
Beschrijving
[read-only]
Datatype
integer
Alias
- UMLS CUI [1]
- C0449438
Beschrijving
[read-only]
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0443172
Beschrijving
[hidden]
Datatype
integer
Alias
- UMLS CUI [1]
- C0184806
Beschrijving
[hidden]
Datatype
date
Alias
- UMLS CUI [1]
- C4321540
Beschrijving
[hidden]
Datatype
date
Alias
- UMLS CUI [1]
- C1115441
Beschrijving
[hidden]
Datatype
integer
Alias
- UMLS CUI [1]
- C0184806
Beschrijving
[hidden]
Datatype
date
Alias
- UMLS CUI [1]
- C4321540
Beschrijving
[hidden]
Datatype
date
Alias
- UMLS CUI [1]
- C1115441
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C0947611
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C2826275
Beschrijving
Use SAE Sequence number from the corresponding SAE form (the last item on the form, in the "Non-Clinical" section) [hidden].
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348585
Beschrijving
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Datatype
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
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Endpoint Hospitalisation for unstable angina GSK study Chronic Coronary Heart Disease NCT00799903
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C0035253 (UMLS CUI [1,2])
C3260278 (UMLS CUI [1,3])
C0027051 (UMLS CUI [1,2])
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