ID

26255

Descrizione

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

Keywords

versioni (3)
  1. 24/09/17 24/09/17 -
  2. 13/10/17 13/10/17 -
  3. 23/10/17 23/10/17 -
Titolare del copyright

GlaxoSmithKline

Caricato su

13 ottobre 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

Inglese

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli  
Pharmacogenetic (PGx) research consent / Blood sample collection
Descrizione

Pharmacogenetic (PGx) research consent / Blood sample collection

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

Informed consent

Tipo di dati

boolean

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

Informed consent date

Tipo di dati

date

Has sample been collected for PGx research?
Descrizione

Answer only if informed consent was obtained for PGx research.

Tipo di dati

boolean

If yes, record date sample taken
Descrizione

date sample taken

Tipo di dati

date

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

reason absence informed consent

Tipo di dati

text

If other reason, specify:
Descrizione

reason absence informed consent specification

Tipo di dati

text

Ritorna all'inizio della pagina

Similar models

Pharmacogenetic research GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

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