ID

26691

Beschrijving

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

Trefwoorden

  1. 24-09-17 24-09-17 -
  2. 13-10-17 13-10-17 -
  3. 23-10-17 23-10-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

23 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Pharmacogenetic (PGx) research consent / Blood sample collection
Beschrijving

Pharmacogenetic (PGx) research consent / Blood sample collection

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

Informed consent

Datatype

boolean

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

Informed consent date

Datatype

date

Has sample been collected for PGx research?
Beschrijving

Answer only if informed consent was obtained for PGx research.

Datatype

boolean

If yes, record date sample taken
Beschrijving

date sample taken

Datatype

date

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

reason absence informed consent

Datatype

text

If other reason, specify:
Beschrijving

reason absence informed consent specification

Datatype

text

Similar models

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
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

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