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Taking people in RussiaNo phase

Tests a heart procedure to prevent irregular heartbeat after heart surgery

Tests a radiofrequency heart procedure to prevent atrial fibrillation after heart surgery.

Plain-language title generated from the registry record
Registry title: Prophylactic Radiofrequency Left Atrial Posterior Wall Isolation to Prevent Atrial Fibrillation After Cardiac Surgery

Key facts

Where
Moscow, RussiaSee the site

Where in Russia

  • Department of Cardiac Surgery, Yudin HospitalMoscow, RussiaTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Vasily I. Kaleda
Trial code
NCT06823778
Record updated
21 February 2025
Original description
The goal of this clinical trial is to learn if an epicardial radiofrequency left atrial posterior wall isolation (box lesion ablation) prevents atrial fibrillation after cardiac surgery. The main question it aims to answer is:Read full original descriptionShow less

Prophylactic Radiofrequency Left Atrial Posterior Wall Isolation (box Lesion Ablation) to Prevent Atrial Fibrillation After Cardiac Surgery (PROBOX): a Randomized Controlled Trial

The goal of this clinical trial is to learn if an epicardial radiofrequency left atrial posterior wall isolation (box lesion ablation) prevents atrial fibrillation after cardiac surgery. The main question it aims to answer is:

- Does box lesion ablation lower the number of patients experiencing de-novo atrial fibrillation requiring any treatment after cardiac surgery? Researchers will compare box lesion ablation to no ablation to see if ablation prevents postoperative atrial fibrillation.

Participants will undergo ablation or no ablation at the time of other cardiac surgery.

Data will be collected while in hospital. Additional information will be collected on 30th day after surgery by telephone call or during a visit.

Inclusion: All patients undergoing cardiac surgery by a single surgeon (V.K.); Informed consent.

Exclusion: Off-pump surgery; Emergent/salvage surgery; History of atrial fibrillation/flutter; Minimally invasive approach; Severe pericardial adhesions.

ClinicalTrials.gov NCT06823778