ID

26172

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: Survival

Mots-clés

  1. 10/10/2017 10/10/2017 -
  2. 10/10/2017 10/10/2017 -
  3. 16/10/2017 16/10/2017 -
  4. 16/10/2017 16/10/2017 -
  5. 23/10/2017 23/10/2017 -
  6. 11/01/2018 11/01/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

10 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Survival GSK study Chronic Coronary Heart Disease NCT00799903

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

Survival data
Description

Survival data

1. Subject status
Description

Subject status

Type de données

integer

If subject known to be alive: Subject known to be alive on (date)
Description

Date Subject known to be alive

Type de données

date

If subject known to be alive: Source of information
Description

Subject alive Source of information

Type de données

text

If subject died: date that site acquired death information
Description

date that site acquired death information

Type de données

date

If subject died: Source of information
Description

death of subject Source of information

Type de données

text

If no new Survival Status data available: Date of most recent attempt to assess survival status
Description

Date of most recent attempt to assess survival status

Type de données

date

Similar models

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Survival data
Item
1. Subject status
integer
Code List
1. Subject status
CL Item
Subject known to be alive (1)
CL Item
Subject died (2)
CL Item
No new Survival Status data available for this subject since the last data were collected (3)
Date Subject known to be alive
Item
If subject known to be alive: Subject known to be alive on (date)
date
Item
If subject known to be alive: Source of information
text
Code List
If subject known to be alive: Source of information
CL Item
Health care provider other than investigative site staff (1)
CL Item
Family member (2)
CL Item
Publicly available information (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
CL Item
Other (OT)
date that site acquired death information
Item
If subject died: date that site acquired death information
date
Item
If subject died: Source of information
text
Code List
If subject died: Source of information
CL Item
Health care provider other than investigative site staff (1)
CL Item
Family member (2)
CL Item
Publicly available information (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
CL Item
Other (OT)
Date of most recent attempt to assess survival status
Item
If no new Survival Status data available: Date of most recent attempt to assess survival status
date

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