Informatie: This is an outdated version of the data model. You can find a Versions overview via Versions on the left. You can find the newest Version by clicking here.
Informatie:
Fout:
ID
5592
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT00168051
Link
http://clinicaltrials.gov/show/NCT00168051
Trefwoorden
Versies (4)
- 12/5/11 12/5/11 - Philipp Bruland
- 4/13/14 4/13/14 - Julian Varghese
- 8/10/14 8/10/14 - Martin Dugas
- 9/20/21 9/20/21 -
Geüploaded op
August 10, 2014
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility NCT00168051 Hemophilia A
Similar models
Eligibility
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
18 Years to 64 Years
boolean
C0001779 (UMLS CUI-1)
Male
Item
Male
boolean
C0024554 (UMLS CUI-1)
Hemophilia A
Item
Severe hemophilia A
boolean
C0019069 (UMLS CUI-1)
Treatment with Factor VIII
Item
Previously treated patients with at least 150 exposure days to any Factor VIII product
boolean
C0087111 (UMLS CUI-1)
C0015506 (UMLS CUI-2)
C0015506 (UMLS CUI-2)
Hypersensitivity Factor VIII
Item
Hypersensitivity to any recombinant Factor VIII product
boolean
C0020517 (UMLS CUI-1)
C0015506 (UMLS CUI-2)
C0015506 (UMLS CUI-2)
Factor VIII inhibitor
Item
History of or current Factor VIII inhibitor
boolean
C0368953 (UMLS CUI-1)
Bleeding episode
Item
Bleeding episode or other reason requiring Factor VIII treatment within 3 days of study
boolean
C0005779 (UMLS CUI-1)