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Assessing AThrough Radiofrequency Transseptal Puncture System for Left Atrial Access

Atrial Fibrillation Clinical Trial

Official title:
A Prospective, Multicenter, Randomized Controlled, Non-inferiority Clinical Study Evaluating the Safety and Efficacy of the AThrough Radiofrequency Transseptal Puncture System in Atrial Septal Puncture.

Clinical Trial Summary

This study is a prospective, multicenter, randomized controlled trial with a non-inferiority design. Participants are patients scheduled for atrial septal puncture. After signing informed consent, subjects will be randomly assigned to either the radiofrequency transseptal puncture system group (referred to as the trial group) or the traditional mechanical transseptal puncture system group (referred to as the control group). All participants will undergo immediate postoperative and discharge clinical follow-ups.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06386458
Study type Interventional
Source Hangzhou NOYA MedTech Co. Ltm.
Contact
Status Completed
Phase N/A
Start date July 8, 2022
Completion date May 11, 2023
View Details
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