ID

26691

Descrição

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: Pharmacogenetic research

Palavras-chave

Versões (3)
  1. 24/09/2017 24/09/2017 -
  2. 13/10/2017 13/10/2017 -
  3. 23/10/2017 23/10/2017 -
Titular dos direitos

GlaxoSmithKline

Transferido a

23 de outubro de 2017

DOI

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Licença

Creative Commons BY-NC 3.0
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Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Inglês

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulários  
Pharmacogenetic (PGx) research consent / Blood sample collection
Descrição

Pharmacogenetic (PGx) research consent / Blood sample collection

1. Has informed consent been obtained for PGx research?
Descrição

Informed consent

Tipo de dados

boolean

If yes, record: Date informed consent obtained for PGx research
Descrição

Informed consent date

Tipo de dados

date

Has sample been collected for PGx research?
Descrição

Answer only if informed consent was obtained for PGx research.

Tipo de dados

boolean

If yes, record date sample taken
Descrição

date sample taken

Tipo de dados

date

If no informed consent for PGx research was obtained, check reason
Descrição

reason absence informed consent

Tipo de dados

text

If other reason, specify:
Descrição

reason absence informed consent specification

Tipo de dados

text

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Similar models

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Pharmacogenetic (PGx) research consent / Blood sample collection
Informed consent
Item
1. Has informed consent been obtained for PGx research?
boolean
Informed consent date
Item
If yes, record: Date informed consent obtained for PGx research
date
sample collection
Item
Has sample been collected for PGx research?
boolean
date sample taken
Item
If yes, record date sample taken
date
Item
If no informed consent for PGx research was obtained, check reason
text
reason absence informed consent
Code List
If no informed consent for PGx research was obtained, check reason
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other (Z)
reason absence informed consent specification
Item
If other reason, specify:
text
Voltar ao início da página 

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