ID

28409

Beschreibung

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

Stichworte

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Rechteinhaber

GlaxoSmithKline

Hochgeladen am

11. Januar 2018

DOI

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Lizenz

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

Englisch

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare  
Survival data
Beschreibung

Survival data

1. Subject status
Beschreibung

Subject status

Datentyp

integer

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

Date Subject known to be alive

Datentyp

date

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

Subject alive Source of information

Datentyp

text

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

date that site acquired death information

Datentyp

date

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

death of subject Source of information

Datentyp

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
Beschreibung

Date of most recent attempt to assess survival status

Datentyp

date

Alias
UMLS CUI [1]
C3846084
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Ähnliche Modelle

Survival Identification GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
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