ID

28408

Description

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: End of study Survival status

Keywords

Versions (4)
  1. 10/10/17 10/10/17 -
  2. 10/16/17 10/16/17 -
  3. 10/23/17 10/23/17 -
  4. 1/11/18 1/11/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

January 11, 2018

DOI

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License

Creative Commons BY-NC 3.0
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End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

English

End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 forms  
Assessment date
Description

Assessment date

1. Most recent survival status assessment
Description

Most recent survival status assessment

Data type

date

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C3846084
Survival data
Description

Survival data

1. Subject status
Description

Subject status

Data type

integer

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

Date Subject known to be alive

Data type

date

Alias
UMLS CUI [1,1]
C3274947
UMLS CUI [1,2]
C0805839
If subject known to be alive: Source of information
Description

Subject alive Source of information

Data type

text

Alias
UMLS CUI [1]
C0807975
If subject known to be alive: Other source of information, specify
Description

Subject alive Source of information specification

Data type

text

Alias
UMLS CUI [1,1]
C2584946
UMLS CUI [1,2]
C0807975
If subject died: date that site acquired death information
Description

date that site acquired death information

Data type

date

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

death of subject Source of information

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1955348
If subject died: Other source of information, specify
Description

Subject dead Source of information specification

Data type

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1955348
UMLS CUI [1,3]
C2348235
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Similar models

End of study Survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Assessment date
Most recent survival status assessment
Item
1. Most recent survival status assessment
date
C2985720 (UMLS CUI [1,1])
C3846084 (UMLS CUI [1,2])
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)
Date Subject known to be alive
Item
If subject known to be alive: Subject known to be alive on (date)
date
C3274947 (UMLS CUI [1,1])
C0805839 (UMLS CUI [1,2])
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 (3)
C1955348 (UMLS CUI-1)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
CL Item
Investigative site staff (4)
C0018724 (UMLS CUI-1)
(Comment:en)
CL Item
Friend or neighbor (5)
C0079382 (UMLS CUI-1)
(Comment:en)
Subject alive Source of information specification
Item
If subject known to be alive: Other source of information, specify
text
C2584946 (UMLS CUI [1,1])
C0807975 (UMLS CUI [1,2])
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 (3)
C1955348 (UMLS CUI-1)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
CL Item
Investigative site staff (4)
C0018724 (UMLS CUI-1)
(Comment:en)
CL Item
Friend or neighbor (5)
C0079382 (UMLS CUI-1)
(Comment:en)
Subject dead Source of information specification
Item
If subject died: Other source of information, specify
text
C0011065 (UMLS CUI [1,1])
C1955348 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
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