Informações:
Falhas:
ID
23469
Descrição
Ibutilide Administration During Pulmonary Vein Ablation; ODM derived from: https://clinicaltrials.gov/show/NCT00589992
Link
https://clinicaltrials.gov/show/NCT00589992
Palavras-chave
Versões (1)
- 06/07/2017 06/07/2017 -
Transferido a
6 de julho de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00589992
Eligibility Atrial Fibrillation NCT00589992
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT00589992
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Thermoablation Atrial Fibrillation Scheduled
Item
patients to be scheduled for atrial fibrillation radio frequency ablation
boolean
C0441476 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0004238 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
Paroxysmal atrial fibrillation | Permanent atrial fibrillation Symptomatic | Conventional Treatment Refractory
Item
paroxysmal, permanent symptomatic atrial fibrillation refractory to conventional treatment
boolean
C0235480 (UMLS CUI [1])
C2586056 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C2945704 (UMLS CUI [3,1])
C0205269 (UMLS CUI [3,2])
C2586056 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C2945704 (UMLS CUI [3,1])
C0205269 (UMLS CUI [3,2])
ATRIAL FIBRILLATION SYMPTOMATIC | Medication refused | Electric Countershock Unwilling
Item
symptomatic atrial fibrillation that do not want or desire to take medication or undergo cardioversion
boolean
C0741283 (UMLS CUI [1])
C1319048 (UMLS CUI [2])
C0013778 (UMLS CUI [3,1])
C0558080 (UMLS CUI [3,2])
C1319048 (UMLS CUI [2])
C0013778 (UMLS CUI [3,1])
C0558080 (UMLS CUI [3,2])
Anti-Arrhythmia Agents To be stopped | Amiodarone Excluded
Item
patients on antiarrhythmics that can be discontinued 5 half lifes prior to the procedure except for amiodarone
boolean
C0003195 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
C0002598 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C1272691 (UMLS CUI [1,2])
C0002598 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Hemorrhage Major
Item
patients with recent major hemorrhage (within 6 months)
boolean
C0019080 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,2])
Blood Coagulation Disorders
Item
patients with a coagulopathy
boolean
C0005779 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
patients who are pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Congestive heart failure
Item
patients with acute congestive heart failure
boolean
C0018802 (UMLS CUI [1])
Hypokalemia | Hyperkalemia
Item
patients with hypokalemia or hyperkalemia
boolean
C0020621 (UMLS CUI [1])
C0020461 (UMLS CUI [2])
C0020461 (UMLS CUI [2])
Prolonged QTc
Item
patients with a prolonged qtc > 440mms
boolean
C1969409 (UMLS CUI [1])
Polymorphic ventricular tachycardia Secondary to Anti-Arrhythmia Agents Class
Item
patients with polymorphic ventricular tachycardia secondary to antiarrhythmic class iii and class i
boolean
C0344432 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0003195 (UMLS CUI [1,3])
C0456387 (UMLS CUI [1,4])
C0175668 (UMLS CUI [1,2])
C0003195 (UMLS CUI [1,3])
C0456387 (UMLS CUI [1,4])
Ventricular Dysfunction, Left
Item
patients with left ventricular dysfunction < 40%
boolean
C0242698 (UMLS CUI [1])
Myocardial Infarction
Item
patients with a history of recent mi (< 1 month)
boolean
C0027051 (UMLS CUI [1])
Angioplasty
Item
patients with a history of an angioplasty of < 1 month
boolean
C0162577 (UMLS CUI [1])
Coronary Artery Bypass Surgery
Item
patients with a history of coronary artery bypass grafting surgery of < 3 months.
boolean
C0010055 (UMLS CUI [1])
Kidney Failure, Chronic | Creatinine clearance measurement
Item
patients with a history of chronic renal failure or a creatinine clearance of < 30ml/m
boolean
C0022661 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
C0373595 (UMLS CUI [2])
Cerebrovascular accident
Item
patients with a history of stroke of < 6 months
boolean
C0038454 (UMLS CUI [1])