ID

28290

Descripción

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

Palabras clave

Versiones (5)
  1. 12/10/17 12/10/17 -
  2. 16/10/17 16/10/17 -
  3. 23/10/17 23/10/17 -
  4. 2/1/18 2/1/18 -
  5. 2/1/18 2/1/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

2 de enero de 2018

DOI

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Licencia

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

Inglés

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios  
Assessment date
Descripción

Assessment date

1. Most recent survival status assessment
Descripción

Most recent survival status assessment date

Tipo de datos

date

Alias
UMLS CUI [1]
C3846084
Survival data
Descripción

Survival data

2. Subject status
Descripción

Subject status

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348568
If subject known to be alive: Subject known to be alive on (date):
Descripción

Subject known to be alive date

Tipo de datos

date

Alias
UMLS CUI [1]
C3274947
If subject known to be alive: Source of information
Descripción

Subject alive Source of information

Tipo de datos

text

Alias
UMLS CUI [1]
C0807975
Other source of information, specify
Descripción

Subject alive Other Source of information

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C0449416
UMLS CUI [1,3]
C1533716
UMLS CUI [1,4]
C0038952
If subject died: date that site acquired death information
Descripción

Date that site acquired death information

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1306577
UMLS CUI [1,2]
C1533716
If subject died: Source of information
Descripción

Subject dead Source of information

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0683836
UMLS CUI [1,2]
C0011065
Other source of information, specify
Descripción

Subject dead Other Source of information

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0683836
UMLS CUI [1,2]
C0011065
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Similar models

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Assessment date
Most recent survival status assessment date
Item
1. Most recent survival status assessment
date
C3846084 (UMLS CUI [1])
Item Group
Survival data
Item
2. Subject status
integer
C2348568 (UMLS CUI [1])
Subject status
Code List
2. Subject status
CL Item
Subject known to be alive (1)
C2584946 (UMLS CUI-1)
(Comment:en)
CL Item
Subject died (2)
C0011065 (UMLS CUI-1)
(Comment:en)
Subject known to be alive date
Item
If subject known to be alive: Subject known to be alive on (date):
date
C3274947 (UMLS CUI [1])
Item
If subject known to be alive: Source of information
text
C0807975 (UMLS CUI [1])
Subject alive Source of information
Code List
If subject known to be alive: Source of information
CL Item
Investigative site staff (4)
C1512698 (UMLS CUI-1)
C0205197 (UMLS CUI-2)
C0281588 (UMLS CUI-3)
(Comment:en)
CL Item
Health care provider other than investigative site staff (1)
C0018724 (UMLS CUI-1)
(Comment:en)
CL Item
Family member (2)
C0086282 (UMLS CUI-1)
(Comment:en)
CL Item
Friend or neighbor (5)
C3842310 (UMLS CUI-1)
(Comment:en)
CL Item
Publicly available information (3)
C1546437 (UMLS CUI-1)
C0005957 (UMLS CUI-2)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
Subject alive Other Source of information
Item
Other source of information, specify
text
C0027361 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
C1533716 (UMLS CUI [1,3])
C0038952 (UMLS CUI [1,4])
Date that site acquired death information
Item
If subject died: date that site acquired death information
date
C1306577 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
Item
If subject died: Source of information
text
C0683836 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
Subject alive Source of information
Code List
If subject died: Source of information
CL Item
Investigative site staff (4)
(Comment:en)
CL Item
Health care provider other than investigative site staff (1)
C0018724 (UMLS CUI-1)
(Comment:en)
CL Item
Family member (2)
C0086282 (UMLS CUI-1)
(Comment:en)
CL Item
Friend or neighbor (5)
C0079382 (UMLS CUI-1)
(Comment:en)
CL Item
Publicly available information (3)
C1955348 (UMLS CUI-1)
(Comment:en)
CL Item
Other (OT)
(Comment:en)
Subject dead Other Source of information
Item
Other source of information, specify
text
C0683836 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
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