ID

26691

Beskrivning

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

Nyckelord

  1. 2017-09-24 2017-09-24 -
  2. 2017-10-13 2017-10-13 -
  3. 2017-10-23 2017-10-23 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

23 oktober 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

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
Beskrivning

Pharmacogenetic (PGx) research consent / Blood sample collection

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

Informed consent

Datatyp

boolean

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

Informed consent date

Datatyp

date

Has sample been collected for PGx research?
Beskrivning

Answer only if informed consent was obtained for PGx research.

Datatyp

boolean

If yes, record date sample taken
Beskrivning

date sample taken

Datatyp

date

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

reason absence informed consent

Datatyp

text

If other reason, specify:
Beskrivning

reason absence informed consent specification

Datatyp

text

Similar models

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial