ID

28296

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: End of study Telephone contact

Trefwoorden

Versies (4)
  1. 12-10-17 12-10-17 -
  2. 13-10-17 13-10-17 -
  3. 23-10-17 23-10-17 -
  4. 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 :

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

End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

Engels

End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
End of study contact form
Beschrijving

End of study contact form

1. Was subject contacted?
Beschrijving

subject contact

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332158
UMLS CUI [1,2]
C0681850
Type of contact
Beschrijving

Type of contact

Datatype

integer

Alias
UMLS CUI [1]
C0332158
If telephone: Time of contact
Beschrijving

Time of contact

Datatype

time

Alias
UMLS CUI [1]
C1320531
If telephone: Site staff who conducted call
Beschrijving

ensure documented in source notes

Datatype

text

Alias
UMLS CUI [1]
C0302186
If telephone: Reason why visit was not perfomed in the clinic
Beschrijving

Reason visit was not perfomed in clinic

Datatype

text

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C3838685
Other, specify
Beschrijving

Reason visit was not perfomed in clinic specification

Datatype

text

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C3838685
UMLS CUI [1,3]
C0545082
Terug naar het begin van de pagina

Similar models

End of study Telephone contact GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
End of study contact form
subject contact
Item
1. Was subject contacted?
boolean
C0332158 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
Item
Type of contact
integer
C0332158 (UMLS CUI [1])
Type of contact
Code List
Type of contact
CL Item
Clinic visit (1)
CL Item
Telephone (2)
Time of contact
Item
If telephone: Time of contact
time
C1320531 (UMLS CUI [1])
Item
If telephone: Site staff who conducted call
text
C0302186 (UMLS CUI [1])
Site staff who conducted call
Code List
If telephone: Site staff who conducted call
CL Item
Physician (34)
CL Item
Nurse (35)
CL Item
Other (OT)
Item
If telephone: Reason why visit was not perfomed in the clinic
text
C0566251 (UMLS CUI [1,1])
C3838685 (UMLS CUI [1,2])
Reason visit was not perfomed in clinic
Code List
If telephone: Reason why visit was not perfomed in the clinic
CL Item
Subject refused (1)
C1705116 (UMLS CUI-1)
(Comment:en)
CL Item
Subject not able to visit clinic (2)
C3838685 (UMLS CUI-1)
C0545082 (UMLS CUI-2)
(Comment:en)
CL Item
Other (OT)
C0205394 (UMLS CUI-1)
(Comment:en)
Reason visit was not perfomed in clinic specification
Item
Other, specify
text
C0566251 (UMLS CUI [1,1])
C3838685 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
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