Impact of breathing methods on heart procedure success for atrial fibrillation
The Effect of Mechanical Ventilation on Radiofrequency Ablation in The Treatment of Atrial Fibrillation.
This study tests whether using different breathing methods during a heart procedure for atrial fibrillation can help improve the success of the treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Kocaeli City Hospital Government |
| Locations | 1 site (Kocaeli) |
| Trial ID | NCT06791915 on ClinicalTrials.gov |
What this trial studies
This observational study investigates how different mechanical ventilation techniques during radiofrequency ablation (RFA) for atrial fibrillation (AF) affect procedural outcomes. It focuses on the relationship between catheter stability, contact force, and respiratory motion, which can influence the effectiveness of the ablation. Patients diagnosed with AF who are scheduled for RFA under general anesthesia will be monitored to assess the impact of controlled versus spontaneous ventilation on the success of the procedure. The study aims to optimize techniques to improve energy delivery and reduce AF recurrence rates.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old diagnosed with atrial fibrillation who are scheduled for radiofrequency ablation under general anesthesia.
Not a fit: Patients undergoing ablation under sedation or local anesthesia will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the effectiveness of atrial fibrillation treatments, leading to better patient outcomes and reduced recurrence rates.
How similar studies have performed: Previous studies have indicated that controlled ventilation can improve outcomes in similar procedures, suggesting a promising avenue for further exploration.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosed with atrial fibrillation * planned to receive radiofrequency ablation treatment under general anesthesia * all patients over 18 years of age Exclusion Criteria: \- Patients undergoing ablation under sedation and/or local anesthesia
Where this trial is running
Kocaeli
- Kocaeli City Hospital — Kocaeli, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Merve Yazici Kara
- Email: merreset@hotmail.com
- Phone: +90 533 686 0156
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.