ID

26232

Descrição

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

Palavras-chave

  1. 12/10/2017 12/10/2017 -
  2. 16/10/2017 16/10/2017 -
  3. 23/10/2017 23/10/2017 -
  4. 02/01/2018 02/01/2018 -
  5. 02/01/2018 02/01/2018 -
Titular dos direitos

GlaxoSmithKline

Transferido a

12 de outubro de 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

Assessment date
Descrição

Assessment date

1. Most recent survival status assessment
Descrição

Most recent survival status assessment date

Tipo de dados

date

Survival data
Descrição

Survival data

2. Subject status
Descrição

Subject status

Tipo de dados

integer

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

Subject known to be alive date

Tipo de dados

date

If subject known to be alive: Source of information
Descrição

Subject alive Source of information

Tipo de dados

text

Other source of information, specify
Descrição

Subject alive Other Source of information

Tipo de dados

text

If subject died: date that site acquired death information
Descrição

Date that site acquired death information

Tipo de dados

date

If subject died: Source of information
Descrição

Subject dead Source of information

Tipo de dados

text

Other source of information, specify
Descrição

Subject dead Other Source of information

Tipo de dados

text

Similar models

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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
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
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
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
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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