Viewing Study NCT06573853



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06573853
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-09

Brief Title: Outcomes of PFA Vs RFA for Patients with PSVT a Retrospective and Propensity Score Matching Study
Sponsor: None
Organization: None

Study Overview

Official Title: The Safety and Efficiency of Pulsed Field Ablation and Radiofrequency Ablation in the Treatment of Paroxysmal Supraventricular Tachycardiaa Retrospective and Propensity Score Matching Study
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PFARFAPSVT
Brief 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None