Vsling™ III: Clinical Evaluation of the Vsling™ Device for Ventricular Repair in Patients with Heart Failure

NCT ID: NCT06002386

Last Updated: 2025-01-03

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-31
• Study Completion Date: 2029-12-31

Brief Summary

Prospective, multi-center, open-label clinical study of the feasibility and initial safety and performance of the Vsling™ in patients with heart failure (HF) with evidence of reduced left ventricular ejection fraction, associated with ventricular dilation.

Conditions

HFrEF - Heart Failure with Reduced Ejection Fraction

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DEVICE_FEASIBILITY
• Blinding Strategy: NONE

Study Groups

Vsling device

Vsling device implantation

Group Type: EXPERIMENTAL

Vsling

Intervention Type: DEVICE

Implantable ventricular repair device

Interventions

Vsling

Implantable ventricular repair device

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age≥ 18 and < 85 years

2. Left ventricular end diastolic diameter is greater than or equal to 55mm

3. Ejection fraction ≥20% and ≤40%

4. FMR grade ≤ 2+ (≤ mild FMR) as defined by the guidelines of the American society of echocardiography (via a transthoracic or transesophageal echo)

5. End-systolic Interpapillary muscle distance ≥ 20mm

6. NYHA class II-IVa

7. Cardiomyopathy of ischemic or non-ischemic origins

8. Understands the nature of the study and procedure and able to provide written informed consent

Exclusion Criteria

1. Any evidence of structural (chordal or leaflet) mitral lesions

2. Ventricular tachycardia or ventricular fibrillation within 6 months prior to inclusion in this study

3. Prior mitral valve repair or replacement

4. ICD/CRT/cardiac pacemaker leads implanted within 3 months prior to inclusion in this study

5. Clinical signs of cardiogenic shock within 30 days prior to inclusion in this study

6. Anatomy that, in the opinion of the interventionalist, prevents safe passage of the Vsling™ catheter(s).

7. Severe aortic stenosis

8. Severe, massive, or torrential tricuspid regurgitation requiring surgical or transcatheter repair

9. Known fixed pulmonary hypertension with PA systolic pressure >70 mmHg not responsive to vasodilator therapy

10. ST segment elevation myocardial infarction within 30 days prior to inclusion in this study

11. Congenital heart disease (except PFO, PDA or ASD)

12. Heart Failure due to confirmed amyloid or other restrictive cardiomyopathies

13. Chronic renal insufficiency defined by Creatinine ≥ 3.0 mg/dL or chronic renal replacement therapy

14. Any therapeutic invasive cardiac procedure within 30 days prior to inclusion in the study

15. Any cardiac surgery, within 3 months prior to inclusion in the study

16. Cerebrovascular Accident (CVA) within 90 days prior to inclusion in this study

17. Thrombocytopenia (Platelet count< 100,000/mm3) or thrombocytosis (Platelet count > 750,000/mm3)

18. Body temperature >38°C within 3 days prior to index procedure

19. Bleeding disorders or hypercoagulable state

20. Active peptic ulcer or active gastrointestinal (GI) bleeding within 90 days of the scheduled implant

21. Contraindication to anticoagulants or antiplatelet agents

22. Known allergy to stainless steel, nickel, titanium or contrast agents that cannot be adequately pre-medicated

23. Known hypersensitivity or contraindication to procedural medications which cannot be adequately managed medically

24. Currently participating in another investigational drug or device study that has not completed the primary endpoint or that clinically interferes with the endpoints of this study

25. Co-morbid condition(s) that, in the opinion of the Investigator, limit life expectancy to < 12 months

26. Co-morbid condition(s) that, in the opinion of the investigator, could limit the patient's ability to participate in the study, including compliance with follow-up requirements, or that could impact the scientific integrity of the study

27. Pregnancy

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cardiac Success

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Iris Yadin-Herling

Role: CONTACT

iris.yh@cardiacsuccess.com

972546633352

Other Identifiers

CL-9022

Identifier Type: -

Identifier Source: org_study_id