Outcomes of PFA Vs. RFA for Patients with PSVT: a Retrospective and Propensity Score Matching Study
Launched by CAIJIE SHEN · Aug 26, 2024
Trial Information
Current as of July 24, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying two different treatments for a heart condition called paroxysmal supraventricular tachycardia (PSVT), which causes the heart to beat very fast for short periods. The researchers want to find out if a newer treatment called pulsed field ablation (PFA) is more effective and safer than the traditional method called radiofrequency ablation (RFA). To do this, they will look at the experiences of patients who had either treatment about a year ago and compare their outcomes.
To be eligible for this study, participants need to be between 18 and 80 years old and have PSVT symptoms, such as certain types of fast heart rhythms. They also must be willing to attend follow-up appointments over the next year for tests and evaluations. Participants will receive care and monitoring, and their progress will be tracked at several points over the year. It's important to note that people with certain heart conditions, previous surgeries, or specific health issues may not qualify for this trial. This study aims to provide valuable information about the best treatment options for PSVT.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients with symptomatic PSVT including: atrioventricular nodal re-entrant tachycardia (AVNRT), atrioventricular re-entrant tachycardia (AVRT);
- • 2. Age range: 18 years old ≤ age ≤ 80 years old, with no gender restriction;
- • 3. Willing to receive the examinations and testings during one year follow-up required by the protocol;
- • 4. Voluntary signed informed consent.
- Exclusion Criteria:
- • 1. Organic heart disease;
- • 2. History of cardiac surgery;
- • 3. Previous failed ablation of PSVT;
- • 4. Presence of any implants, such as a permanent pacemaker;
- • 5. Patients with invasive systemic infections or advanced malignant tumors;
- • 6. Contraindications for septal puncture or retrograde transaortic access surgery;
- • 7. Any condition that makes the use of heparin or aspirin inappropriate;
- • 8. Pregnant or lactating women;
- • 9. Inability to fully comply with the study procedures and follow-ups or to provide their own informed consent;
- • 10. Coexistence with other arrhythmias, such as atrial fibrillation.
About Caijie Shen
Caijie Shen is a dedicated clinical trial sponsor focused on advancing medical research and therapeutic development. With a commitment to innovation and patient-centered care, Caijie Shen collaborates with leading research institutions and healthcare professionals to design and implement rigorous clinical studies. The organization prioritizes adherence to regulatory standards and ethical practices, ensuring the integrity and reliability of trial outcomes. By fostering partnerships and leveraging cutting-edge methodologies, Caijie Shen aims to contribute significantly to the advancement of healthcare solutions and improved patient outcomes.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Ningbo, Zhejiang, China
Patients applied
Trial Officials
Caijie Shen
Study Director
First Affiliated Hospital of Ningbo University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported