Informatie:
Fout:
ID
33332
Beschrijving
Investigation on Appropriate Duration of Dabigatran Use After Catheter Ablation for Paroxysmal Atrial Fibrillation in Patients With Low Thromboembolic Risk; ODM derived from: https://clinicaltrials.gov/show/NCT02313584
Link
https://clinicaltrials.gov/show/NCT02313584
Trefwoorden
Versies (1)
- 05-12-18 05-12-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
5 december 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02313584
Eligibility Atrial Fibrillation NCT02313584
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT02313584
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Paroxysmal atrial fibrillation | Catheter ablation
Item
paroxysmal af undergoing catheter ablation
boolean
C0235480 (UMLS CUI [1])
C0162563 (UMLS CUI [2])
C0162563 (UMLS CUI [2])
CHA2DS2-VASc score
Item
cha2ds2-vasc score <= 1
boolean
C4049268 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Persistent atrial fibrillation
Item
persistent af
boolean
C2585653 (UMLS CUI [1])
CHA2DS2-VASc score
Item
cha2ds2-vasc score > 2
boolean
C4049268 (UMLS CUI [1])
Cerebrovascular accident
Item
prior cva
boolean
C0038454 (UMLS CUI [1])
Anticoagulants
Item
prior atnicoagulant
boolean
C0003280 (UMLS CUI [1])
Heart failure Severe
Item
severe hf
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Liver Dysfunction | Abnormal renal function
Item
abnormal liver or renal function
boolean
C0086565 (UMLS CUI [1])
C0151746 (UMLS CUI [2])
C0151746 (UMLS CUI [2])
Hemorrhage Severe
Item
history of severe bleeding
boolean
C0019080 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])