ID

28409

Beskrivning

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

Nyckelord

  1. 2017-10-10 2017-10-10 -
  2. 2017-10-10 2017-10-10 -
  3. 2017-10-16 2017-10-16 -
  4. 2017-10-16 2017-10-16 -
  5. 2017-10-23 2017-10-23 -
  6. 2018-01-11 2018-01-11 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

11 januari 2018

DOI

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Licens

Creative Commons BY-NC 3.0

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Survival GSK study Chronic Coronary Heart Disease NCT00799903

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

Survival data
Beskrivning

Survival data

1. Subject status
Beskrivning

Subject status

Datatyp

integer

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

Date Subject known to be alive

Datatyp

date

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

Subject alive Source of information

Datatyp

text

Alias
UMLS CUI [1]
C0807975
If subject died: date that site acquired death information
Beskrivning

date that site acquired death information

Datatyp

date

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

death of subject Source of information

Datatyp

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
Beskrivning

Date of most recent attempt to assess survival status

Datatyp

date

Alias
UMLS CUI [1]
C3846084

Similar models

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Survival data
Item
1. Subject status
integer
C2348568 (UMLS CUI [1])
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])
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])
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])

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