Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07006493

REFINE-HCM: Intramyocardial Septal Radiofrequency Ablation for Obstructive Hypertrophic Cardiomyopathy

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Capital Medical University Affiliated Beijing Anzhen Hospital, Beijing, Beijing Municipality, China

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 80 years, regardless of sex
  • Diagnosed with obstructive hypertrophic cardiomyopathy (oHCM)
  • Presence of significant symptoms (e.g., dyspnea, chest pain, fatigue, palpitations, syncope)
  • NYHA class II or higher with LVOTG ≥50 mmHg at rest or provoked (assessed by echocardiography)
  • Septal thickness ≥15 mm
  • Unsuitable for surgical myectomy or refusal of surgery
  • Provided informed consent and agree to complete follow-up

Exclusion criteria

  • Asymptomatic or non-obstructive HCM
  • Septal thickness ≥30 mm
  • Mitral valve anatomy not suitable for ablation as judged by investigator
  • High risk of sudden cardiac death (SCD) requiring ICD implantation
  • Complete right bundle branch block at screening
  • Infective endocarditis, myocarditis, atrial myxoma, or intracardiac thrombus
  • Contraindication to transseptal access (e.g., septal patch)
  • Mechanical valves or history of aortic valve replacement
  • Severe heart failure with persistent symptoms and LVEF <40%
  • Major cardiac events within 6 months (e.g., cardiac arrest, MI, heart failure hospitalization)
  • Significant structural heart disease requiring surgery
  • Prior septal reduction therapy or pacemaker implantation
  • Constrictive pericarditis or significant congenital heart disease
  • Bleeding disorders or contraindication to antithrombotic therapy
  • Liver dysfunction (ALT/AST >3× ULN)
  • Renal insufficiency (creatinine >2.0 mg/dL or on dialysis)
  • Pregnant, breastfeeding, or planning pregnancy within 6 months post-op
  • Life expectancy <12 months
  • Participation in other investigational studies within 30 days or 5 half-lives
  • Investigator determines poor compliance or unsuitability
  • Contraindications to cardiac MRI (e.g., ICD, allergy to contrast, claustrophobia)

Treatment and study plan

Transcatheter Intramyocardial Septal Radiofrequency Ablation System

Device

The device system includes a single-use RF ablation catheter, sheath, RF generator, and irrigation pump. Ablation is guided by intracardiac echocardiography (ICE).

Primary outcomes

  1. Treatment Effectiveness Rate at 6 Months

    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.

Secondary outcomes

  1. Change in Resting LVOT Gradient

    Time frame: Baseline, 6 months, 12 months

    Measured by echocardiography at baseline, 6 months, and 12 months

  2. Change in NYHA Functional Class

    Time frame: Baseline, 6 months, 12 months

    Proportion of patients with improvement of ≥1 NYHA class

  3. Change in 6-Minute Walk Distance

    Time frame: Baseline, 6 months, 12 months

    Distance walked in 6 minutes, compared to baseline

  4. Change in 12-Item Short Form Health Survey (SF-12) Score

    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.

  5. Device Success Rate

    Time frame: Day of procedure

    Defined as successful completion of RF ablation per protocol

  6. Incidence of Adverse Events

    Time frame: Through 12 months

    All adverse events related to device or procedure

Study contacts

Contact information is provided by the study sponsor or research team.

Yongxin Su

CONTACT

[email protected]

+86 18121015668

Sponsors and collaborators

Lead sponsor

SuZhou Sinus Medical Technologies Co.,Ltd

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jun 5, 2025
Registry last updated
Dec 15, 2025

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.

Published trials that share one or more normalized conditions with this study.