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The Clinical Research of the Safety and Effectiveness Evaluation for Using Echocardiography-guided Liwen RF Radiofrequency Ablation System to Treat Hypertrophic Obstructive Cardiomyopathy

Primary Purpose

Hypertrophic Obstructive Cardiomyopathy

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Echocardiography-guided Radiofrequency ablation for Hypertrophic obstructive Cardiomyopathy (HOCM).
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertrophic Obstructive Cardiomyopathy focused on measuring Cardiomyopathy, hypertrophic;techniques; Treatment outcome

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subject has pressure gradient of left ventricular outflow tract (LVOT) ≥50 mmHg(with Systolic Anterior Motion)in the resting-state or after exercise stress test.
  2. Subject with obvious clinical symptoms.
  3. Subject with New York Heart Association (NYHA) cardiac function ≥ II grade.
  4. Subject with adequate drug treatment is not effective or cannot tolerate side effects of the drug.
  5. Subject was informed of the nature of the clinical study and agreed to participate in all the requirements of the clinical study, signed an informed consent form, and agreed to complete the following checks.

Exclusion Criteria:

  1. Subject is pregnant, lactating, or planned to conceive during a clinical study.
  2. Subject with Hypertrophic Non-obstructive Cardiomyopathy.
  3. Subject with interventricular septal thickness ≥ 30mm.
  4. Subject with Sudden Cardiac Death Index ≥ 10%.
  5. Subject combined with other heart diseases requires surgical treatment.
  6. Subject with heart failure(Defined as resting heart failure after intensive anti-heart failure therapy, left ventricular fraction of ejecting< 40%).

Sites / Locations

  • Ultrasound Medicine Department of Xijing Hospital, Fourth Military Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hypertrophic Obstructive Cardiomyopathy

Arm Description

Outcomes

Primary Outcome Measures

Main adverse event
Any instrument or surgery-related complications, including but not limited to death, emergency surgery, severe pericardial tamponade requiring pericardiocentesis or surgery, bleeding, surgery-related stroke.

Secondary Outcome Measures

Instrument success
Radiofrequency ablation system instruments reach the desired treatment site and successfully complete ablation,and remove the system successfully.
Operation success
Improvement of LVOTG > 50% within 90 days after operation
No main adverse events related to instruments or surgery within 90 days of instrument use
Life quality score of SF-36
The life quality score of SF-36 was significantly improved after the operation.

Full Information

First Posted
April 17, 2020
Last Updated
January 12, 2021
Sponsor
Xijing Hospital
Collaborators
Hangzhou Nuo Cheng Medical Instrument Co.,Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT04355260
Brief Title
The Clinical Research of the Safety and Effectiveness Evaluation for Using Echocardiography-guided Liwen RF Radiofrequency Ablation System to Treat Hypertrophic Obstructive Cardiomyopathy
Official Title
To Evaluate the Safety and Effectiveness Evaluation of Using Echocardiography-guided Liwen RF Radiofrequency Ablation System to Treat Hypertrophic Obstructive Cardiomyopathy
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 30, 2019 (Actual)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
July 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Xijing Hospital
Collaborators
Hangzhou Nuo Cheng Medical Instrument Co.,Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objective to investigate the safety and effectiveness of Echocardiography-guided radiofrequency ablation in patients with Hypertrophic obstructive Cardiomyopathy (HOCM). Percutaneous intramyocardial septal radiofrequency ablation (Liwen Procedure) is a safe and effective treatment approach for Hypertrophic obstructive Cardiomyopathy and results in sustained improvement in exercise capacity, persistent in reducing Left Ventricle Outflow Tract (LVOT) gradient, and sustained improvement in cardiac function. In patients with disabling symptoms caused by Hypertrophic obstructive Cardiomyopathy (HOCM),Echocardiography-guided radiofrequency ablation could be a less invasive treatment option. Percutaneous intramyocardial septal radiofrequency ablation (Liwen Procedure) is a new method for the diagnosis or treatment of heart disease by using a special diagnosis and treatment device to the heart target area under the guidance of image technology. The method breaks through the worldwide problem of the minimally invasive diagnosis and treatment of the myocardium on the beating heart, so as to avoid the X-ray radiation and contrast agent damage . As a new pathway of cardiac disease intervention, Liwen Procedure can be used in congenital heart disease, myocardial biopsies, drug injection, cell implantation and instrument implantation in addition to Hypertrophic Cardiomyopathy and cardiac tumors. It has important clinical value and broad application prospect. In this study, Liwen RF radiofrequency ablation system was used to treat HOCM , and evaluate its safety and effectiveness , in order to provide a new medical device for Liwen Procedure of HOCM.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Obstructive Cardiomyopathy
Keywords
Cardiomyopathy, hypertrophic;techniques; Treatment outcome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hypertrophic Obstructive Cardiomyopathy
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Echocardiography-guided Radiofrequency ablation for Hypertrophic obstructive Cardiomyopathy (HOCM).
Intervention Description
Echocardiography-guided Radiofrequency ablation for Hypertrophic obstructive Cardiomyopathy (HOCM).
Primary Outcome Measure Information:
Title
Main adverse event
Description
Any instrument or surgery-related complications, including but not limited to death, emergency surgery, severe pericardial tamponade requiring pericardiocentesis or surgery, bleeding, surgery-related stroke.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Instrument success
Description
Radiofrequency ablation system instruments reach the desired treatment site and successfully complete ablation,and remove the system successfully.
Time Frame
30 days
Title
Operation success
Description
Improvement of LVOTG > 50% within 90 days after operation
Time Frame
90 days
Title
No main adverse events related to instruments or surgery within 90 days of instrument use
Time Frame
90 days
Title
Life quality score of SF-36
Description
The life quality score of SF-36 was significantly improved after the operation.
Time Frame
90 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject has pressure gradient of left ventricular outflow tract (LVOT) ≥50 mmHg(with Systolic Anterior Motion)in the resting-state or after exercise stress test. Subject with obvious clinical symptoms. Subject with New York Heart Association (NYHA) cardiac function ≥ II grade. Subject with adequate drug treatment is not effective or cannot tolerate side effects of the drug. Subject was informed of the nature of the clinical study and agreed to participate in all the requirements of the clinical study, signed an informed consent form, and agreed to complete the following checks. Exclusion Criteria: Subject is pregnant, lactating, or planned to conceive during a clinical study. Subject with Hypertrophic Non-obstructive Cardiomyopathy. Subject with interventricular septal thickness ≥ 30mm. Subject with Sudden Cardiac Death Index ≥ 10%. Subject combined with other heart diseases requires surgical treatment. Subject with heart failure(Defined as resting heart failure after intensive anti-heart failure therapy, left ventricular fraction of ejecting< 40%).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liwen Liu, MD
Phone
86-13571975528
Email
liuliwencrt@hotmail.com
Facility Information:
Facility Name
Ultrasound Medicine Department of Xijing Hospital, Fourth Military Medical University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
LiWen Liu, MD
Phone
86-13571975528

12. IPD Sharing Statement

Citations:
PubMed Identifier
33628143
Citation
Han C, Zhou M, Hu R, Wang B, Zuo L, Li J, Ta S, Hsi DH, Liu J, Wei L, Liu L. Trans-Septal Myocardial Biopsy in Hypertrophic Cardiomyopathy Using the Liwen Procedure: An Introduction of a Novel Technique. J Interv Cardiol. 2021 Feb 10;2021:1905184. doi: 10.1155/2021/1905184. eCollection 2021.
Results Reference
derived

Learn more about this trial

The Clinical Research of the Safety and Effectiveness Evaluation for Using Echocardiography-guided Liwen RF Radiofrequency Ablation System to Treat Hypertrophic Obstructive Cardiomyopathy

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