ID
43663
Beschrijving
Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atrial Fibrillation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02168829
Link
https://clinicaltrials.gov/show/NCT02168829
Trefwoorden
Versies (2)
- 25-04-16 25-04-16 -
- 20-09-21 20-09-21 -
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02168829
Eligibility Atrial Fibrillation NCT02168829
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Negation Inclusion
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1518422
- UMLS CUI [1,2]
- C1512693
Beschrijving
Unable Informed Consent
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1299582
- UMLS CUI [1,2]
- C0021430
Beschrijving
Study Subject Participation Status
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
Glomerular Filtration Rate
Datatype
boolean
Alias
- UMLS CUI [1]
- C0017654
Beschrijving
Medical contraindication Oral anticoagulants
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0354604
Beschrijving
Metallic Heart Valve Prosthesis
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0018825
- UMLS CUI [1,2]
- C2986473
Beschrijving
Disease Requirement Long-term oral anticoagulants
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1514873
- UMLS CUI [1,3]
- C0354604
- UMLS CUI [1,4]
- C0443252
Beschrijving
Cerebrovascular accident
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038454
Similar models
Eligibility Atrial Fibrillation NCT02168829
- StudyEvent: Eligibility
C0004238 (UMLS CUI [1,2])
C0162563 (UMLS CUI [2,1])
C0225860 (UMLS CUI [2,2])
C0003811 (UMLS CUI [2,3])
C0004239 (UMLS CUI [3])
C0001779 (UMLS CUI [2])
C0086287 (UMLS CUI [3,1])
C0042373 (UMLS CUI [3,2])
C1512693 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0354604 (UMLS CUI [1,2])
C2986473 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,2])
C0354604 (UMLS CUI [1,3])
C0443252 (UMLS CUI [1,4])