ID

26232

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: Third party survival status

Keywords

versioni (5)
  1. 12/10/17 12/10/17 -
  2. 16/10/17 16/10/17 -
  3. 23/10/17 23/10/17 -
  4. 02/01/18 02/01/18 -
  5. 02/01/18 02/01/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

12 ottobre 2017

DOI

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Licenza

Creative Commons BY-NC 3.0
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Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

Inglese

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli  
Assessment date
Descrizione

Assessment date

1. Most recent survival status assessment
Descrizione

Most recent survival status assessment date

Tipo di dati

date

Survival data
Descrizione

Survival data

2. Subject status
Descrizione

Subject status

Tipo di dati

integer

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

Subject known to be alive date

Tipo di dati

date

If subject known to be alive: Source of information
Descrizione

Subject alive Source of information

Tipo di dati

text

Other source of information, specify
Descrizione

Subject alive Other Source of information

Tipo di dati

text

If subject died: date that site acquired death information
Descrizione

Date that site acquired death information

Tipo di dati

date

If subject died: Source of information
Descrizione

Subject dead Source of information

Tipo di dati

text

Other source of information, specify
Descrizione

Subject dead Other Source of information

Tipo di dati

text

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Similar models

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Assessment date
Most recent survival status assessment date
Item
1. Most recent survival status assessment
date
Item Group
Survival data
Item
2. Subject status
integer
Subject status
Code List
2. Subject status
CL Item
Subject known to be alive (1)
CL Item
Subject died (2)
Subject known to be alive date
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
Subject alive Source of information
Code List
If subject known to be alive: Source of information
CL Item
Investigative site staff (4)
CL Item
Health care provider other than investigative site staff (1)
CL Item
Family member (2)
CL Item
Friend or neighbor (5)
CL Item
Publicly available information (3)
CL Item
Other (OT)
Item
Other source of information, specify
text
Subject alive Source of information
Code List
Other source of information, specify
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
Subject alive Source of information
Code List
If subject died: Source of information
CL Item
Investigative site staff (4)
CL Item
Health care provider other than investigative site staff (1)
CL Item
Family member (2)
CL Item
Friend or neighbor (5)
CL Item
Publicly available information (3)
CL Item
Other (OT)
Subject dead Other Source of information
Item
Other source of information, specify
text
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