ID
28267
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: Cancer Report Form - Repeating form (Scheduled visits)
Palabras clave
Versiones (4)
- 4/10/17 4/10/17 -
- 13/10/17 13/10/17 -
- 23/10/17 23/10/17 -
- 1/1/18 1/1/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
1 de enero de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Cancer Report Form Repeating form GSK study Chronic Coronary Heart Disease NCT00799903
Cancer Report Form Repeating form GSK study Chronic Coronary Heart Disease NCT00799903
Descripción
2. New cancer details
Descripción
Date of diagnosis new cancer
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0205314
- UMLS CUI [1,2]
- C0006826
- UMLS CUI [1,3]
- C0011900
- UMLS CUI [1,4]
- C0011008
Descripción
Site new cancer
Tipo de datos
integer
Descripción
Other site new cancer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0006826
- UMLS CUI [1,2]
- C2945843
Descripción
Other site new cancer specification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0751623
- UMLS CUI [1,2]
- C1515974
- UMLS CUI [1,3]
- C2348235
Descripción
pathology report new cancer
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0807321
Descripción
3. Recurrence of cancer details
Descripción
Date of recurrence
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0277556
Descripción
Site recurrence
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1515974
- UMLS CUI [1,2]
- C0277556
Descripción
Other site recurrence
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1515974
- UMLS CUI [1,2]
- C0277556
Descripción
Other site recurrence specification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1515974
- UMLS CUI [1,2]
- C0277556
- UMLS CUI [1,3]
- C2348235
Descripción
pathology report recurrence
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0807321
Descripción
pathology report primary diagnosis recurrence
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1302656
- UMLS CUI [1,2]
- C0807321
- UMLS CUI [1,3]
- C4291713
Descripción
4. Metastatic cancer details
Descripción
Date of diagnosis of metastasis
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0027627
Descripción
Site of metastasis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0807944
Descripción
Other site metastasis
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0807944
Descripción
Other site specification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C2348235
Descripción
pathology report metastasis
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0807321
Descripción
Date of diagnosis primary site
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2316983
Descripción
Primary site metastasis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0807944
Descripción
Other primary site
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0475447
Descripción
Other primary site specification
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0475447
Descripción
pathology report primary diagnosis metastasis
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1302656
- UMLS CUI [1,2]
- C0807321
- UMLS CUI [1,3]
- C4291713
Descripción
5. Was the subject hospitalised related to this diagnosis?
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