ID

28409

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: Survival

Palabras clave

Versiones (6)
  1. 10/10/17 10/10/17 -
  2. 10/10/17 10/10/17 -
  3. 16/10/17 16/10/17 -
  4. 16/10/17 16/10/17 -
  5. 23/10/17 23/10/17 -
  6. 11/1/18 11/1/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

11 de enero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Survival GSK study Chronic Coronary Heart Disease NCT00799903

Inglés

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios  
Survival data
Descripción

Survival data

1. 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

Date Subject known to be alive

Tipo de datos

date

Alias
UMLS CUI [1]
C2584946
If subject known to be alive: Source of information
Descripción

Subject alive Source of information

Tipo de datos

text

Alias
UMLS CUI [1]
C0807975
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

death of subject Source of information

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1955348
If no new Survival Status data available: Date of most recent attempt to assess survival status
Descripción

Date of most recent attempt to assess survival status

Tipo de datos

date

Alias
UMLS CUI [1]
C3846084
Volver a la parte superior de la página

Similar models

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Survival data
Item
1. Subject status
integer
C2348568 (UMLS CUI [1])
Subject status
Code List
1. 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)
CL Item
No new Survival Status data available for this subject since the last data were collected (3)
C1320722 (UMLS CUI-1)
(Comment:en)
Date Subject known to be alive
Item
If subject known to be alive: Subject known to be alive on (date)
date
C2584946 (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
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
Publicly available information (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
C1955348 (UMLS CUI-1)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
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
C0011065 (UMLS CUI [1,1])
C1955348 (UMLS CUI [1,2])
Subject alive Source of information
Code List
If subject died: Source of information
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
Publicly available information (e.g., newspaper, newsletter, featured in a performance, award, or interview, etc) (3)
C1955348 (UMLS CUI-1)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
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
C3846084 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial