Informatie:
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ID
25895
Beschrijving
Global Anticoagulant Registry in the Field; ODM derived from: https://clinicaltrials.gov/show/NCT01090362
Link
https://clinicaltrials.gov/show/NCT01090362
Trefwoorden
Versies (1)
- 25-09-17 25-09-17 -
Geüploaded op
25 september 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01090362
Eligibility Atrial Fibrillation NCT01090362
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01090362
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Prospective Cohort
Item
prospective cohort
boolean
C1709709 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 18 years and older
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation Newly Diagnosed | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure
Item
new diagnosis of non-valvular atrial fibrillation (diagnosed within the last 6 weeks) with at least one additional risk factor for stroke and regardless of therapy.
boolean
C0004238 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
C1518321 (UMLS CUI [1,2])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
Retrospective Cohort
Item
retrospective validation cohort
boolean
C2985505 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 18 years and older
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure
Item
diagnosis of non-valvular af (diagnosed 6-24 months prior to enrolment) with at least one additional risk factor for stroke and regardless of therapy.
boolean
C0004238 (UMLS CUI [1])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
Follow-up Plan Lacking
Item
no further follow-up envisaged or possible within enrolling hospital or with associated family practitioner.
boolean
C3274571 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Atrial Fibrillation Transitory | Atrial Fibrillation Secondary to Cause Reversible
Item
patients with transient af secondary to a reversible cause.
boolean
C0004238 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0015127 (UMLS CUI [2,3])
C0205343 (UMLS CUI [2,4])
C0205374 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0015127 (UMLS CUI [2,3])
C0205343 (UMLS CUI [2,4])
Patient Recruitment Controlled study
Item
patients recruited in controlled clinical trials.
boolean
C0242800 (UMLS CUI [1,1])
C0681867 (UMLS CUI [1,2])
C0681867 (UMLS CUI [1,2])