ID

28290

Beschrijving

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

Trefwoorden

Versies (5)
  1. 12-10-17 12-10-17 -
  2. 16-10-17 16-10-17 -
  3. 23-10-17 23-10-17 -
  4. 02-01-18 02-01-18 -
  5. 02-01-18 02-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

2 januari 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

Geen commentaren

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

Engels

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
Assessment date
Beschrijving

Assessment date

1. Most recent survival status assessment
Beschrijving

Most recent survival status assessment date

Datatype

date

Alias
UMLS CUI [1]
C3846084
Survival data
Beschrijving

Survival data

2. Subject status
Beschrijving

Subject status

Datatype

integer

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

Subject known to be alive date

Datatype

date

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

Subject alive Source of information

Datatype

text

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

Subject alive Other Source of information

Datatype

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
Beschrijving

Date that site acquired death information

Datatype

date

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

Subject dead Source of information

Datatype

text

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

Subject dead Other Source of information

Datatype

text

Alias
UMLS CUI [1,1]
C0683836
UMLS CUI [1,2]
C0011065
Terug naar het begin van de pagina

Similar models

Third party survival status GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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