ID
28402
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: Liver events
Palabras clave
Versiones (5)
- 11/10/17 11/10/17 -
- 16/10/17 16/10/17 -
- 16/10/17 16/10/17 -
- 23/10/17 23/10/17 -
- 11/1/18 11/1/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
11 de enero de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Liver events GSK study Chronic Coronary Heart Disease NCT00799903
Liver events GSK study Chronic Coronary Heart Disease NCT00799903
Descripción
Liver events
Descripción
subject age
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0001779
Descripción
If yes, ensure Pregnancy Notification Form has been completed.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0549206
Descripción
diagnostic imaging of liver or hepatobiliary system
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1711359
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [1,3]
- C0023884
Descripción
If No, record the details on the Non-Serious Adverse Events form or Serious Adverse Event form.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1711359
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [1,3]
- C0023884
- UMLS CUI [1,4]
- C1254595
Descripción
If yes, complete Liver Biopsy form.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0193388
Descripción
If yes, record on the appropriate Concomitant Medication form.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0002346
- UMLS CUI [1,2]
- C0242295
- UMLS CUI [1,3]
- C0281875
Descripción
dietary change
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3671772
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2985767
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Liver events GSK study Chronic Coronary Heart Disease NCT00799903
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C0023884 (UMLS CUI [1,3])
C1254595 (UMLS CUI [1,4])
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