ID
28345
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 revascularisation - Repeating form (Scheduled visits)
Mots-clés
Versions (4)
- 07/10/2017 07/10/2017 -
- 16/10/2017 16/10/2017 -
- 23/10/2017 23/10/2017 -
- 05/01/2018 05/01/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
5 janvier 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
Description
Urgent coronary revascularisation for myocardial ischemia
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C3260278
Description
criteria for urgent coronary revscularisation for myocardial ischemia not met
Type de données
text
Alias
- UMLS CUI [1,1]
- C0151744
- UMLS CUI [1,2]
- C0948089
Description
Non-urgent coronary revascularisation
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0877341
- UMLS CUI [1,2]
- C0543467
Description
Revascularisation was a treatment for MI
Type de données
boolean
Description
[hidden]
Type de données
text
Description
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Type de données
integer
Alias
- UMLS CUI [1]
- C0243095
Description
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Type de données
integer
Alias
- UMLS CUI [1]
- C1317081
Description
Acute MI
Type de données
text
Alias
- UMLS CUI [1]
- C0155626
Description
prior MI
Type de données
text
Alias
- UMLS CUI [1]
- C1275835
Description
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C1536220
- UMLS CUI [2]
- C3537184
Description
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C1305738
Description
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C1275835
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1]
- C3260278
Description
CEC Status
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C1444748
Description
[read-only]
Type de données
integer
Alias
- UMLS CUI [1]
- C0449438
Description
[read-only]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0443172
Description
[hidden]
Type de données
integer
Alias
- UMLS CUI [1]
- C0031831
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2082575
- UMLS CUI [1,3]
- C1519246
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0184806
- UMLS CUI [1,2]
- C1115441
Description
[hidden]
Type de données
integer
Alias
- UMLS CUI [1]
- C0031831
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1]
- C3166278
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0184806
- UMLS CUI [1,2]
- C1115441
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
[hidden]
Type de données
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].
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348585
Description
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Type de données
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
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Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
C1301880 (UMLS CUI [1,2])
C1532338 (UMLS CUI-2)
(Comment:en)
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C1272704 (UMLS CUI-2)
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C0856737 (UMLS CUI [1,2])
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C0856737 (UMLS CUI [1,2])
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C2825200 (UMLS CUI [1,2])
C1262327 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C2183050 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,2])
C0035253 (UMLS CUI [1,2])
C1532338 (UMLS CUI [1,2])
C0745417 (UMLS CUI [1,3])
C1532338 (UMLS CUI [1,2])
C0745417 (UMLS CUI [1,3])
C2065834 (UMLS CUI [1,4])
C0035253 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
(Comment:en)
C3897171 (UMLS CUI-2)
(Comment:en)
C0948089 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C3537184 (UMLS CUI [2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0027051 (UMLS CUI-2)
(Comment:en)
C0151744 (UMLS CUI-2)
(Comment:en)
(Comment:en)
C1956346 (UMLS CUI-2)
(Comment:en)
C0020649 (UMLS CUI-2)
(Comment:en)
C0023211 (UMLS CUI-2)
(Comment:en)
(Comment:en)
C0443172 (UMLS CUI [1,2])
C2082575 (UMLS CUI [1,2])
C1519246 (UMLS CUI [1,3])
C1115441 (UMLS CUI [1,2])
C1115441 (UMLS CUI [1,2])
C2348585 (UMLS CUI [1,2])
C2826934 (UMLS CUI [1,2])