Transcatheter Intramyocardial Septal Radiofrequency Ablation System
DeviceThe device system includes a single-use RF ablation catheter, sheath, RF generator, and irrigation pump. Ablation is guided by intracardiac echocardiography (ICE).
NCT Number: NCT07006493
This is a prospective, multicenter, randomized, parallel-controlled, superiority clinical trial designed to evaluate the efficacy and safety of a transcatheter intramyocardial septal radiofrequency ablation system for the treatment of patients with obstructive hypertrophic cardiomyopathy (oHCM). Eligible participants will be randomized in a 2:1 ratio to receive either active ablation under intracardiac echocardiographic guidance or a sham procedure. All participants will continue to receive standard-of-care medical therapy during the study period. The primary endpoint is the treatment effectiveness rate at 6 months, defined as a ≥50% reduction in LVOT gradient from baseline or a resting LVOT gradient <30 mmHg.
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Not applicable
Capital Medical University Affiliated Beijing Anzhen Hospital, Beijing, Beijing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The device system includes a single-use RF ablation catheter, sheath, RF generator, and irrigation pump. Ablation is guided by intracardiac echocardiography (ICE).
Time frame: 6 months post-procedure
Defined as either (1) a ≥50% reduction in resting LVOT gradient from baseline, or (2) resting LVOT gradient <30 mmHg.
Time frame: Baseline, 6 months, 12 months
Measured by echocardiography at baseline, 6 months, and 12 months
Time frame: Baseline, 6 months, 12 months
Proportion of patients with improvement of ≥1 NYHA class
Time frame: Baseline, 6 months, 12 months
Distance walked in 6 minutes, compared to baseline
Time frame: Baseline, 6 months, 12 months
The SF-12 Health Survey includes two components: the Physical Component Summary (PCS) and the Mental Component Summary (MCS). Scores range from 0 to 100, with higher scores indicating better health status.
Time frame: Day of procedure
Defined as successful completion of RF ablation per protocol
Time frame: Through 12 months
All adverse events related to device or procedure
Contact information is provided by the study sponsor or research team.
SuZhou Sinus Medical Technologies Co.,Ltd
Industry
A Prospective, Multicenter, Randomized, Parallel-Controlled Superiority Study Evaluating the Efficacy and Safety of a Transcatheter Intramyocardial Septal Radiofrequency Ablation System in Patients With Obstructive Hypertrophic Cardiomyopathy
Acronym: REFINE-HCM
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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