ID

25875

Description

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: Pharmagogenetic research

Mots-clés

Versions (3)
  1. 24/09/2017 24/09/2017 -
  2. 13/10/2017 13/10/2017 -
  3. 23/10/2017 23/10/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

24 septembre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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Pharmagogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

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Pharmagogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires  
Pharmacogenetic (PGx) research consent / Blood sample collection
Description

Pharmacogenetic (PGx) research consent / Blood sample collection

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

Informed consent

Type de données

boolean

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

Informed consent date

Type de données

date

Has sample been collected for PGx research?
Description

Answer only if informed consent was obtained for PGx research.

Type de données

boolean

If yes, record date sample taken
Description

date sample taken

Type de données

date

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

reason absence informed consent

Type de données

text

If other reason, specify:
Description

reason absence informed consent specification

Type de données

text

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Similar models

Pharmagogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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
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