ID
28345
Descripción
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)
Palabras clave
Versiones (4)
- 7/10/17 7/10/17 -
- 16/10/17 16/10/17 -
- 23/10/17 23/10/17 -
- 5/1/18 5/1/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
5 de enero de 2018
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
Descripción
Urgent coronary revascularisation for myocardial ischemia
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3260278
Descripción
criteria for urgent coronary revscularisation for myocardial ischemia not met
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0151744
- UMLS CUI [1,2]
- C0948089
Descripción
Non-urgent coronary revascularisation
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0877341
- UMLS CUI [1,2]
- C0543467
Descripción
Revascularisation was a treatment for MI
Tipo de datos
boolean
Descripción
[hidden]
Tipo de datos
text
Descripción
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0243095
Descripción
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1317081
Descripción
Acute MI
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0155626
Descripción
prior MI
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1275835
Descripción
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1536220
- UMLS CUI [2]
- C3537184
Descripción
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1305738
Descripción
As a result of the revascularization, criterion for a peri-procedural MI was met. MI adjudication for event not already reported by investigaton [hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1275835
Descripción
[hidden]
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3260278
Descripción
CEC Status
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1444748
Descripción
[read-only]
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0449438
Descripción
[read-only]
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0443172
Descripción
[hidden]
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0031831
Descripción
[hidden]
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2082575
- UMLS CUI [1,3]
- C1519246
Descripción
[hidden]
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0184806
- UMLS CUI [1,2]
- C1115441
Descripción
[hidden]
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0031831
Descripción
[hidden]
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3166278
Descripción
[hidden]
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0184806
- UMLS CUI [1,2]
- C1115441
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0947611
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826275
Descripción
Use SAE Sequence number from the corresponding SAE form (the last item on the form, in the "Non-Clinical" section) [hidden].
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348585
Descripción
Copy Serious Adverse Event term from corresponding SAE form [hidden].
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
Similar models
Endpoint revascularisation GSK study Chronic Coronary Heart Disease NCT00799903
C1301880 (UMLS CUI [1,2])
C1532338 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C1272704 (UMLS CUI-2)
(Comment:en)
C0856737 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C0856737 (UMLS CUI [1,2])
C2825200 (UMLS CUI [1,2])
C1262327 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
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])