Actively Recruiting
Effect of Mechanical Ventilation on Radiofrequency Ablation in the Treatment of Atrial Fibrillation
Led by Kocaeli City Hospital · Updated on 2025-01-24
50
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the effects of different mechanical ventilation methods on radiofrequency ablation (RFA) treatment for atrial fibrillation (AF). This study focuses on how controlled breathing affects catheter stability and contact force during the procedure, which are crucial for successful energy delivery to heart tissue and long-lasting pulmonary vein isolation (PVI). The trial compares ventilation methods used during general anesthesia to determine their impact on procedural success and AF recurrence. Participants will receive radiofrequency ablation under general anesthesia using one of two mechanical ventilation modes: Flow Controlled Ventilation (FCV) or Volume Controlled Ventilation (VCV). Both methods involve controlled breathing to reduce thoracic movement and improve catheter contact with the heart tissue. The study records ventilation settings, heart and respiratory measurements, and ablation lesion details such as ablation time, contact force, and impedance drop. Clinical outcomes including freedom from arrhythmias and procedural complications will be tracked during follow-up. During the study, participants will undergo monitoring of vital signs and ventilation parameters alongside detailed recording of ablation procedure characteristics. Researchers will measure the duration of the ablation procedure, changes in electrocardiography from baseline, and the rate of atrial fibrillation recurrence one month after the treatment. The study aims to gather data on procedural efficiency and safety, with follow-up evaluations to assess long-term effects. Total ablation time varies between 1 and 3 hours depending on the procedure.
CONDITIONS
Brief Title
Effect of Mechanical Ventilation on Radiofrequency Ablation in Atrial Fibrillation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with atrial fibrillation
- Planned to receive radiofrequency ablation treatment under general anesthesia
- Aged 18 years or older
You will not qualify if you...
- Undergoing ablation under sedation and/or local anesthesia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 to 3 hours
Participants undergo radiofrequency ablation for atrial fibrillation under general anesthesia using either Flow Controlled Mechanical Ventilation (FCV) or Volume Controlled Mechanical Ventilation (VCV).
1 procedure visit (in-person)
Duration - 1 month
Participants are monitored for atrial fibrillation recurrence and procedural complications after the ablation procedure.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
Kocaeli City Hospital
Kocaeli, Turkey (Türkiye)
Actively Recruiting
Research Team
M
Merve Yazici Kara
N
Nurseda Dundar
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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