ID
28449
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)
Mots-clés
Versions (6)
- 07/10/2017 07/10/2017 -
- 16/10/2017 16/10/2017 -
- 23/10/2017 23/10/2017 -
- 11/01/2018 11/01/2018 -
- 14/01/2018 14/01/2018 -
- 20/09/2021 20/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
14 janvier 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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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]
Type de données
text
Alias
- UMLS CUI [1]
- C0680730
Description
criteria for heart failure not met specification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0018801
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]
- C0184806
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Type de données
integer
Alias
- UMLS CUI [1]
- C0184806
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1515023
- UMLS CUI [1,4]
- C0011008
Description
[hidden]
Type de données
date
Alias
- UMLS CUI [1,1]
- C0031831
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C1514756
- UMLS CUI [1,4]
- C0011008
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
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])