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Valveclip® Transcatheter Mitral Valve Repair Study

Primary Purpose

Mitral Regurgitation

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Valveclip® Transcatheter mitral valve repair
Sponsored by
Shanghai NewMed Medical Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mitral Regurgitation

Eligibility Criteria

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

Inclusion Criteria:

  1. Severe mitral regurgitation≥3+ (moderate or above degenerative mitral regurgitation disease, or with stenosis is included);
  2. Age≥70 years; or patients who are 60~70 years old, and the STS risk score indicate that participants are at high risk of traditional surgery or cannot tolerate traditional thoracotomy;

4) Left ventricular ejection fraction≥30%; 5) As assessed by multidisciplinary cardiac team (at least two cardiac surgeons/one cardiologist), patients who are at extremely high-risk or unsuitable for routine mitral valve surgery with evaluation; 6) Patients who understand the purpose of the trial and volunteer to participate in, sign the informed consent form and are willing to accept relevant examinations and clinical follow-ups.

Anatomy selection Criteria:

  1. The regurgitant jet of mitral valve originates from the A2 and P2 (the lesions of A2/P2 in mitral valve causes regurgitation);
  2. The width of the mitral valve prolapsed area is ≤15mm, Height of Prolapse ≤10mm or coaptation depth≤11mm, coaptation height≥2mm, effective length of anterior and posterior leaflets>1cm (conforming to EVEREST II recommended mitral valve interventional edge-to-edge repair standards);
  3. Effective mitral valve orifice area≥ 4.0cm2;
  4. No obvious calcification of the mitral valve annulus and valve leaflets;
  5. Patient's anatomical conditions allow transseptal approach.

Exclusion Criteria:

  1. Previous cardiac mitral valve surgery;
  2. Patients with Infective endocarditis or having an active infection;
  3. Patients with mitral regurgitation caused by pure mitral stenosis;
  4. Combined with untreated severe coronary artery disease
  5. Pulmonary hypertension (pulmonary artery systolic pressure>70mmHg);
  6. Patients with severe right heart failure;
  7. Patients are extremely weak and cannot tolerate general anesthesia or are in shock that circulatory support is needed;
  8. Patients with hypertrophic cardiomyopathy, restrictive cardiomyopathy, and constrictive pericarditis;
  9. Patients receiving chronic dialysis;
  10. Patients with clear coagulation dysfunction and severe coagulopathy;
  11. Patients with clear contraindications to anticoagulant drugs;
  12. Patients with stroke or transient ischemic attack within 30 days;
  13. Echocardiography found any intracardiac mass, left ventricle or atrial thrombus;
  14. Patients who require surgery or interventional therapy for other valvular lesions;
  15. Patients with severe macrovascular lesions requiring surgical treatment;
  16. Patients' imaging examinations suggest that the anatomy of the heart and valves are inappropriate;

Sites / Locations

  • Department of Cardiology, West China Hospital, Sichuan UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

Transcatheter Mitral Valve Repair with Valveclip®

Outcomes

Primary Outcome Measures

Efficacy of product
Efficacy of product is defined as the proportion of participants meeting effective standards after surgery (freedom from death, mitral valve reoperation or MR>2+ at 12 months).

Secondary Outcome Measures

Efficacy of product
Efficacy of product is defined as the proportion of participants meeting effective standards after surgery (freedom from death, mitral valve reoperation or MR>2+ at 30 days, 180 days, 2 to 5 years).
Rate of Cardiovascular related mortality
Cardiovascular related mortality after Transcatheter Mitral Valve Repairment
Rate of Severe adverse events
Severe adverse events after Transcatheter Mitral Valve Repairment (including death, stroke, myocardial infarction, reoperation, instrumental non-selective cardiovascular surgery, renal failure, and adverse events related to transfemoral vein septal approach surgery, etc.)
Quality of life Improvement
The 12-Item Short-Form Health Survey(SF-12)

Full Information

First Posted
August 16, 2021
Last Updated
November 16, 2022
Sponsor
Shanghai NewMed Medical Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05021614
Brief Title
Valveclip® Transcatheter Mitral Valve Repair Study
Official Title
Evaluation of the Efficacy and Safety of the Transcatheter Mitral Valve Repair System in Patients With Moderate and Above Degenerative Mitral Regurgitation at High Surgical Risk
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 24, 2021 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
September 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai NewMed Medical 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
Yes

5. Study Description

Brief Summary
The purpose of this clinical trial is to evaluate the effectiveness and safety of the transcatheter mitral valve repair system in the treatment of patients with moderate or above degenerative mitral regurgitation.
Detailed Description
This study is a prospective,multi-center, single-arm, safety and performance clinical study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mitral Regurgitation

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
Treatment
Arm Type
Experimental
Arm Description
Transcatheter Mitral Valve Repair with Valveclip®
Intervention Type
Device
Intervention Name(s)
Valveclip® Transcatheter mitral valve repair
Intervention Description
Transcatheter mitral valve repair system
Primary Outcome Measure Information:
Title
Efficacy of product
Description
Efficacy of product is defined as the proportion of participants meeting effective standards after surgery (freedom from death, mitral valve reoperation or MR>2+ at 12 months).
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Efficacy of product
Description
Efficacy of product is defined as the proportion of participants meeting effective standards after surgery (freedom from death, mitral valve reoperation or MR>2+ at 30 days, 180 days, 2 to 5 years).
Time Frame
30 days, 180 days, 2 to 5 years
Title
Rate of Cardiovascular related mortality
Description
Cardiovascular related mortality after Transcatheter Mitral Valve Repairment
Time Frame
30 days, 180 days, 1 year, 2 to 5 years
Title
Rate of Severe adverse events
Description
Severe adverse events after Transcatheter Mitral Valve Repairment (including death, stroke, myocardial infarction, reoperation, instrumental non-selective cardiovascular surgery, renal failure, and adverse events related to transfemoral vein septal approach surgery, etc.)
Time Frame
30 days, 180 days, 1 year, 2 to 5 years
Title
Quality of life Improvement
Description
The 12-Item Short-Form Health Survey(SF-12)
Time Frame
30 days, 180 days, 1 year, 2 to 5 years
Other Pre-specified Outcome Measures:
Title
Technical success
Description
Technical success after Transcatheter Mitral Valve Repairment
Time Frame
immediate post-surgical
Title
Device success
Description
Device success after Transcatheter Mitral Valve Repairment
Time Frame
30 days、180 days、1 year
Title
Procedural success
Description
Procedural success after Transcatheter Mitral Valve Repairment
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe mitral regurgitation≥3+ (moderate or above degenerative mitral regurgitation disease, or with stenosis is included); Age≥70 years; or patients who are 60~70 years old, and the STS risk score indicate that participants are at high risk of traditional surgery or cannot tolerate traditional thoracotomy; 4) Left ventricular ejection fraction≥30%; 5) As assessed by multidisciplinary cardiac team (at least two cardiac surgeons/one cardiologist), patients who are at extremely high-risk or unsuitable for routine mitral valve surgery with evaluation; 6) Patients who understand the purpose of the trial and volunteer to participate in, sign the informed consent form and are willing to accept relevant examinations and clinical follow-ups. Anatomy selection Criteria: The regurgitant jet of mitral valve originates from the A2 and P2 (the lesions of A2/P2 in mitral valve causes regurgitation); The width of the mitral valve prolapsed area is ≤15mm, Height of Prolapse ≤10mm or coaptation depth≤11mm, coaptation height≥2mm, effective length of anterior and posterior leaflets>1cm (conforming to EVEREST II recommended mitral valve interventional edge-to-edge repair standards); Effective mitral valve orifice area≥ 4.0cm2; No obvious calcification of the mitral valve annulus and valve leaflets; Patient's anatomical conditions allow transseptal approach. Exclusion Criteria: Previous cardiac mitral valve surgery; Patients with Infective endocarditis or having an active infection; Patients with mitral regurgitation caused by pure mitral stenosis; Combined with untreated severe coronary artery disease Pulmonary hypertension (pulmonary artery systolic pressure>70mmHg); Patients with severe right heart failure; Patients are extremely weak and cannot tolerate general anesthesia or are in shock that circulatory support is needed; Patients with hypertrophic cardiomyopathy, restrictive cardiomyopathy, and constrictive pericarditis; Patients receiving chronic dialysis; Patients with clear coagulation dysfunction and severe coagulopathy; Patients with clear contraindications to anticoagulant drugs; Patients with stroke or transient ischemic attack within 30 days; Echocardiography found any intracardiac mass, left ventricle or atrial thrombus; Patients who require surgery or interventional therapy for other valvular lesions; Patients with severe macrovascular lesions requiring surgical treatment; Patients' imaging examinations suggest that the anatomy of the heart and valves are inappropriate;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
chunyang Wang, CRA
Phone
(86)-21-20788668
Email
cywang@newmed.cn
First Name & Middle Initial & Last Name or Official Title & Degree
xuyang Xie
Phone
(86)-21-20788668
Email
xyxie@newmed.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
mao Chen, Chief
Organizational Affiliation
West China Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiology, West China Hospital, Sichuan University
City
Sichuan
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
mao Chen, Chief

12. IPD Sharing Statement

Plan to Share IPD
No

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Valveclip® Transcatheter Mitral Valve Repair Study

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