Expanded Study of the HighLife 28mm Trans-septal Trans-catheter Mitral Valve in Patients With Moderate-severe or Severe Mitral Regurgitation and at High Surgical Risk

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHighLife SAS

About this trial

to evaluate the safety and performance of the HighLife 28mm transcatheter, trans-septal Mitral Valve in patients with moderate-severe or severe mitral regurgitation who are at high risk for surgical treatment.

Eligibility criteria

Qualifiers

1. Age ≥ 18 years 2. Moderate-severe or severe mitral regurgitation (≥ 3+) 3. Patient has New York Heart Association (NYHA) Functional Class II, III or ambulatory IV 4. Patient is under guideline directed medical therapy, as reviewed and confirmed by the local multidisciplinary Heart Team, for at least one month 5. Patient is high-risk for open-heart surgery based on the assessment of the multidisciplinary Heart Team using standard scoring systems and consideration of co-morbidities, frailty, and disability 6. Patient meets the anatomical criteria for HighLife valve 7. Patient is willing to participate in the study and provides signed informed consent

Disqualifiers

Any stroke/TIA within 30 days

Severe symptomatic carotid stenosis (> 70% by non-invasive imaging)

Active infections requiring antibiotic therapy

Active ulcer or gastro-intestinal bleeding in the past 3 months

Trial design

Treatments tested in this trial

  • HighLife Transcatheter Mitral Valve Replacement

Treatment groups

120 Participants
are divided into 1 treatment group

Sponsors and collaborators

HighLife SAS

Lead sponsor

ICON plc

Collaborator