Saline Enhanced Radiofrequency (SERF) Needle Ablation for Refractory VT

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The Thermedical Ablation System and Durablate catheter is indicated for use in patients with recurrent, sustained, monomorphic ventricular tachycardia (SMVT) refractory to drug therapy and conventional (approved) catheter ablation. Subjects with recurrent, SMVT refractory to drug therapy and conventional catheter ablation who are not eligible for, or will not likely benefit from repeat endocardial ablation using an approved catheter.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Subject has structural heart disease

• Subject has recurrent symptomatic sustained (\> 30 seconds) monomorphic ventricular tachycardia (MMVT) within 180 days prior to planned study ablation that meets the following criteria:

‣ At least 3 episodes of the MMVT have been treated with ATP and/or shock, OR at least 2 episodes were treated with shock AND

⁃ Documentation of the presumed recurrent MMVT was treated with prior catheter ablation AND

⁃ Occurred despite treatment with at least one Class III antiarrhythmic after last ablation or treatment with a Class III antiarrhythmic is not tolerated or is contraindicated AND

⁃ VT has recurred despite VT ablation at one of the investigational centers UORU the investigator documents the reason that the subject is unlikely to benefit from a repeat ablation using a conventional, approved catheter.

• Subject is at least 18 years old

• Subject has an implantable cardioverter-defibrillator (ICD) with a full 6-month (prior to planned study ablation) ICD interrogation history documenting incidences of VT

• Subject is able to provide informed consent

Locations
United States
Alabama
University of Alabama at Birmingham
NOT_YET_RECRUITING
Birmingham
Pennsylvania
Hospital of the University of Pennsylvania
NOT_YET_RECRUITING
Philadelphia
South Carolina
Medical University of South Carolina
NOT_YET_RECRUITING
Charleston
Tennessee
Vanderbilt University Medical Center
NOT_YET_RECRUITING
Nashville
Utah
Intermountain Healthcare
RECRUITING
Salt Lake City
Other Locations
Canada
Montreal Heart Institute - Institut de Cardiologie de Montréal
RECRUITING
Montreal
Quebec Heart and Lung Institute - Institut universitaire de cardiologie et de pneumologie de Québec
NOT_YET_RECRUITING
Québec
Contact Information
Primary
Michael Curley, PhD
mcurley@thermedical.com
617-899-9843
Backup
Mary DeVoe
m.devoe@thermedical.com
Time Frame
Start Date: 2025-08-09
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 130
Treatments
Experimental: Single arm treatment
All subjects meeting inclusion/exclusion criteria and successfully consented will be treated with the study device.
Sponsors
Leads: Thermedical, Inc.

This content was sourced from clinicaltrials.gov