NCT05332691

Brief Summary

The primary purpose of this study is to evaluate the feasibility, the safety and the efficacy of the transapical beating-heart septal myectomy for the treatment of hypertrophic obstructive cardiomyopathy. This is a prospective, single-arm, single-center, first-in-man study.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Apr 2022

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 11, 2022

Completed
4 days until next milestone

Study Start

First participant enrolled

April 15, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 18, 2022

Completed
2.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
Last Updated

November 7, 2024

Status Verified

November 1, 2024

Enrollment Period

2.7 years

First QC Date

April 11, 2022

Last Update Submit

November 5, 2024

Conditions

Keywords

Hypertrophic Obstructive CardiomyopathySeptal MyectomySystolic Anterior MotionLeft Ventricle Outflow Tract ObstructionMitral RegurgitationTransapicalOff-pumpMinimally invasive

Outcome Measures

Primary Outcomes (2)

  • All-cause mortality

    Death from any cause during the observation period.

    3 months

  • Procedural success

    Resting left ventricle outflow tract gradients \< 30 mmHg, provoked left ventricle outflow tract gradients \< 50 mmHg, and mitral regurgitation (MR) ≤ grade 1+.

    3 months

Secondary Outcomes (13)

  • Device success

    1 day

  • Septal thickness

    7 days and 3 months

  • Left ventricle mass

    3 months

  • Left ventricle volume

    7 days and 3 months

  • Cardiac diastolic function

    7 days and 3 months

  • +8 more secondary outcomes

Study Arms (1)

Hypertrophic Obstructive Cardiomyopathy

EXPERIMENTAL

Transapical beating-heart septal myectomy for the patient with hypertrophic obstructive cardiomyopathy.

Procedure: Transapical beating-heart septal myectomy

Interventions

We have invented a beating-heart myectomy device.Through a minimally invasive intercostal incision, septal myectomy could be accomplished via a transapical access in the beating heart using the device. The whole process of resection is monitored, navigated, and evaluated by real-time transesophageal and transthoracic echocardiography. Left ventricle outlet tract gradient and the grade of mitral regurgitation are evaluated each time after resection. Multiple resections are performed to tailor the muscular resection for sufficient relief of left ventricle outlet tract obstruction and mitral regurgitation, while preventing iatrogenic injuries.

Also known as: Minimally invasive transapical septal myectomy in the beating hearts
Hypertrophic Obstructive Cardiomyopathy

Eligibility Criteria

Age8 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients whose resting or provoked left ventricular outflow tract gradient \> 50 mmHg, and maximal ventricular septal wall thickness ≥ 15 mm.
  • Patients with heart function of New York Heart Association ≥ class II.
  • Patients with drug-refractory symptoms or intolerable to pharmaceutical therapies.
  • Patients who was informed the nature of the clinical trial, consented to participate in all of the activities of the clinical trial, and signed the informed consent form.

You may not qualify if:

  • Patients who were pregnant.
  • Patients who had concomitant diseases such as intrinsic valvular disease or coronary artery disease that needed open-heart surgery.
  • Patients who had severe heart failure with left ventricle ejection fraction \< 40%.
  • Patients whose estimated life expectancy \< 12 m.
  • Patient who were non-compliant.
  • Patients under circumstances which were considered not suitable or prohibitive for participating the clinical trial at the discretion of the attending medical team and the researchers.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, 430000, China

RECRUITING

Related Publications (4)

  • Fang J, Wang R, Liu H, Su Y, Chen J, Han X, Wei Y, Chen Y, Cheng L, Wei X. Transapical septal myectomy in the beating heart via a minimally invasive approach: a feasibility study in swine. Interact Cardiovasc Thorac Surg. 2020 Feb 1;30(2):303-311. doi: 10.1093/icvts/ivz249.

    PMID: 31642911BACKGROUND
  • Chen Y, Quintana E, Fang J, Liu Y, Wei X. Transapical Beating-Heart Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy With Anomalous Papillary Muscle Insertion. Interdiscip Cardiovasc Thorac Surg. 2025 Sep 2;40(9):ivaf195. doi: 10.1093/icvts/ivaf195.

  • Fang J, Chen Y, Liu Y, Li R, Zhu Y, Zhou W, Cheng L, Wang Q, Shi J, Wei Y, Ma Y, Quintana E, Grau JB, Wan S, Wei X. Transapical Beating-Heart Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy: Lessons Learned After the Learning Curve Period. Circ Cardiovasc Interv. 2025 May;18(5):e015044. doi: 10.1161/CIRCINTERVENTIONS.124.015044. Epub 2025 May 2.

  • Fang J, Liu Y, Zhu Y, Li R, Wang R, Wang DW, Song Y, Li C, Chen Y, Cheng L, Zheng K, Zhao Y, Li S, Cheng C, Xia L, Chen X, Wan S, Wei X. First-in-Human Transapical Beating-Heart Septal Myectomy in Patients With Hypertrophic Obstructive Cardiomyopathy. J Am Coll Cardiol. 2023 Aug 15;82(7):575-586. doi: 10.1016/j.jacc.2023.05.052.

MeSH Terms

Conditions

Cardiomyopathy, HypertrophicMitral Valve Insufficiency

Condition Hierarchy (Ancestors)

CardiomyopathiesHeart DiseasesCardiovascular DiseasesAortic Stenosis, SubvalvularAortic Valve StenosisAortic Valve DiseaseHeart Valve Diseases

Study Officials

  • Xiang Wei, M.D.

    Tongji Hospital

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Beating-heart myectomy device
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Professor and Director

Study Record Dates

First Submitted

April 11, 2022

First Posted

April 18, 2022

Study Start

April 15, 2022

Primary Completion

December 30, 2024

Study Completion

December 30, 2025

Last Updated

November 7, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will share

All of the conclusive participant data, after removing the individual information of privacy, will be uploaded as supporting information when publishing the current study.

Shared Documents
STUDY PROTOCOL, SAP, CSR
Time Frame
After the current study is published.
Access Criteria
All readers who were interested in the current study.

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