Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06573853

Outcomes of PFA Vs. RFA for Patients with PSVT: a Retrospective and Propensity Score Matching Study

The Safety and Efficiency of Pulsed Field Ablation and Radiofrequency Ablation in the Treatment of Paroxysmal Supraventricular Tachycardia:a Retrospective and Propensity Score Matching Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
428 (estimated)
Sponsor
Caijie Shen · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The goal of this retrospective study is to compare the long-term follow-up outcomes of pulses field ablation (PFA) Vs. radiofrequency ablation (RFA) for the patients with paroxysmal supraventricular tachycardia (PSVT). The main question to answer is: Does the PFA was more effecient and safer that RFA for treatment of PSVT during procedure and after 1-year follow-up? Researchers will compare the acute and long-term efficiency and safety between PFA and RFA. 1. Recieved PFA or RFA 1 year ago 2. Finish the visit to the clinic at 1, 3, 6, 12 months for examinations and blood testings 3. Patients recieved PFA and PFA under propensity matched comparison according to differen variety of PSVT

Detailed description

The goal of this retrospective study is to compare the long-term follow-up outcomes of PFA Vs. RFA for the patients with PSVT. The main question to answer is: Does the PFA was more effecient and safer that RFA for treatment of PSVT during procedure and after 1-year follow-up? Researchers will compare the acute and long-term efficiency and safety between PFA and RFA.

Conditions

Interventions

TypeNameDescription
PROCEDUREFocal Pulsed Field Ablation (PFA)Patients in the PFA group underwent ablation procedures utilizing a force-sensing PFA catheter for the treatment of PSVT.
PROCEDUREFocal Radiofrequecy Ablation (RFA)Patients in the PFA group underwent ablation procedures utilizing force-sensing RFA catheters for the treatment of PSVT.

Timeline

Start date
2022-10-11
Primary completion
2025-06-30
Completion
2025-06-30
First posted
2024-08-27
Last updated
2024-10-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06573853. Inclusion in this directory is not an endorsement.