ID

26738

Beschrijving

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

Trefwoorden

Versies (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 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

23 oktober 2017

DOI

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Licentie

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

Engels

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
Assessment date
Beschrijving

Assessment date

1. Most recent survival status assessment
Beschrijving

Most recent survival status assessment date

Datatype

date

Survival data
Beschrijving

Survival data

2. Subject status
Beschrijving

Subject status

Datatype

integer

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

Subject known to be alive date

Datatype

date

If subject known to be alive: Source of information
Beschrijving

Subject alive Source of information

Datatype

text

Other source of information, specify
Beschrijving

Subject alive Other Source of information

Datatype

text

If subject died: date that site acquired death information
Beschrijving

Date that site acquired death information

Datatype

date

If subject died: Source of information
Beschrijving

Subject dead Source of information

Datatype

text

Other source of information, specify
Beschrijving

Subject dead Other Source of information

Datatype

text

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Similar models

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Terug naar het begin van de pagina 

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