ID

26116

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 Withdrawal of consent

Trefwoorden

  1. 09-10-17 09-10-17 -
  2. 16-10-17 16-10-17 -
  3. 23-10-17 23-10-17 -
  4. 11-01-18 11-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

9 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Pharmacogenetic research Withdrawal of consent GSK study Chronic Coronary Heart Disease NCT00799903

Pharmacogenetic research Withdrawal of consent Subject Identification GSK study Chronic Coronary Heart Disease NCT00799903

Withdrawal of consent for PGx (DNA) / Blood sample destruction
Beschrijving

Withdrawal of consent for PGx (DNA) / Blood sample destruction

1. Has subject withdrawn consent for PGx research?
Beschrijving

withdrawal consent for PGx research

Datatype

boolean

If subject has withdrawn consent for PGx research: date informed consent withdrawn
Beschrijving

date informed consent withdrawn

Datatype

date

2. Has a request been made for blood sample destruction?
Beschrijving

request for blood sample destruction

Datatype

boolean

If a request has been made for blood sample destruction, check reason
Beschrijving

request for blood sample destruction reason

Datatype

text

If other reason applied, specify
Beschrijving

request for blood sample destruction other reason

Datatype

text

Similar models

Pharmacogenetic research Withdrawal of consent Subject Identification GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Withdrawal of consent for PGx (DNA) / Blood sample destruction
withdrawal consent for PGx research
Item
1. Has subject withdrawn consent for PGx research?
boolean
date informed consent withdrawn
Item
If subject has withdrawn consent for PGx research: date informed consent withdrawn
date
request for blood sample destruction
Item
2. Has a request been made for blood sample destruction?
boolean
Item
If a request has been made for blood sample destruction, check reason
text
Code List
If a request has been made for blood sample destruction, check reason
CL Item
Subject withdrew consent for PGx (3)
CL Item
Other (Z)
request for blood sample destruction other reason
Item
If other reason applied, specify
text

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