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Recruiting NCT06253000

NCT06253000 Radiofrequency and Cryoablation of the Posterior Wall of the Left Atrium

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Clinical Trial Summary
NCT ID NCT06253000
Status Recruiting
Phase
Sponsor Bakulev Scientific Center of Cardiovascular Surgery
Condition Stroke
Study Type INTERVENTIONAL
Enrollment 158 participants
Start Date 2023-06-10
Primary Completion 2025-12-30

Trial Parameters

Condition Stroke
Sponsor Bakulev Scientific Center of Cardiovascular Surgery
Study Type INTERVENTIONAL
Phase N/A
Enrollment 158
Sex ALL
Min Age 18 Years
Max Age 80 Years
Start Date 2023-06-10
Completion 2025-12-30
Interventions
CryoablationRadiofrequency ablation

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Brief Summary

Atrial fibrillation (AF) is the cause of 20% of strokes, and the risk of stroke in a person suffering from this arrhythmia increases by 5 times. Ischemic stroke in patients with AF is often fatal and, compared with stroke of other etiology, leads to the most pronounced disability and more often recurs. Accordingly, the risk of death in patients with AF-related stroke is 2 times higher, and treatment costs increase 1.5 times. The main interventional method of treating AF, available in most medical institutions, is the use of radio frequency and/or cryoenergy to eliminate destructive damage to the left atrium (LA). The aim of this study is to compare two different interventional methods and identify predictors of recurrence in patients with persistent and long-term AF.

Eligibility Criteria

Inclusion Criteria: * Age over 18 years old; * Atrial fibrillation resistant to antiarrhythmic therapy; * Persistent and long-persisting form of atrial fibrillation; * The patient's consent to participate in the study. Exclusion Criteria: * Age under 18 and over 80 years old; * The presence of another cardiac pathology requiring surgical treatment; * Congenital heart defects; * Previous "open" cardiac surgery; * Bone marrow diseases; * Pathology of the blood coagulation system; * The left ventricular ejection fraction is less than 40%; * Moderate to severe renal insufficiency (creatinine clearance \<50 ml/min); * Drug-resistant hypertension (despite hypotensive therapy); * Organically altered mitral valve; * There are reasons to assume that the patient will not show up for subsequent visits (control points of the study) for various reasons; * The patient's participation in another clinical trial.

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