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Clinical Trials in the UK / NCT02322840
Active, not recruiting Not applicable

Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early Feasibility Study of the TMVR Transseptal System

NCT02322840 · tracked via the Priya Life Science UK tracker
Sponsor
Medtronic Cardiovascular
Phase
Not applicable
Started
2015-04
Last updated
2026-01-14

Condition(s) studied

Mitral Valve Insufficiency

Investigational drug(s) / intervention(s)

Twelve TMVR ImplantMedtronic Intrepid™ Transcatheter Transfemoral Mitral Valve Replacement System

Twelve TMVR Implant: Implantation of the Twelve TMVR System - Apical

Medtronic Intrepid™ Transcatheter Transfemoral Mitral Valve Replacement System: Implantation of the Medtronic Intrepid™ Transcatheter Mitral Valve- Transfemoral

Study summary

PILOT:

The study is a pilot trial to evaluate the safety and performance of the Twelve TMVR System in high risk mitral regurgitation patients.

EFS:

The study is an Early Feasibility Study to evaluate the safety and performance of the Medtronic Intrepid™ Transcatheter Mitral Valve Replacement System with Transfemoral Transseptal access in Patients with moderate-Severe or severe, Symptomatic Mitral Regurgitation

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * Severe mitral regurgitation (PILOT) * moderate-severe or severe mitral regurgitation (EFS) * Symptomatic mitral regurgitation (NYHA Class II-IV) * Deemed to be at high risk for conventional mitral valve surgery by the local heart team (including, at minimum, a cardiac surgeon, interventional cardiologist, and an echocardiologist) (PILOT and EFS) * Subjects anatomically suitable for the Intrepid TMVR delivery system, including transfemoral and transseptal access (EFS only) * Native mitral valve geometry and size compatible with the Intrepid™ TMVR (PILOT) Key Exclusion Criteria: * Left ventricular ejection fraction (LVEF) \< 20 (PILOT) or \<30% (EFS) * Evidence of intracardiac mass, thrombus, or vegetation * Prior valve surgery or need for other valve surgery * Prior stroke within 30 days (PILOT) or 90 days (EFS) * Gastrointestinal bleeding within 6 months (PILOT) * Prior myocardial infarction 90 days (EFS) * Need for coronary revascularization * History of, or active, endocarditis if antibiotics are required (EFS) * Renal insufficiency; Serum Creatinine \> 2.5 mg/dL (PILOT) or Creatinine Clearance \<30 cc/min (EFS)

Primary outcome measure(s)

Trial sites (32)

FacilityCityRegionStatus
Abrazo Arizona Heart Hospital - EFS Phoenix Arizona
Cedars-Sinai Medical Center - PILOT Los Angeles California
Piedmont Atlanta Hospital - PILOT Atlanta Georgia
Northwestern Memorial Hospital - PILOT Chicago Illinois
University of Michigan Health System - University Hospital - PILOT Ann Arbor Michigan
Corewell Health - EFS Grand Rapids Michigan
Abbott Northwestern Hospital - EFS Minneapolis Minnesota
Abbott Northwestern Hospital - PILOT Minneapolis Minnesota
Barnes Jewish Hospital - PILOT St Louis Missouri
NYU Langone Medical Center - PILOT New York New York
The Mount Sinai Hospital (New York NY) - EFS New York New York
The Mount Sinai Hospital (New York NY) - PILOT New York New York
New York-Presbyterian Hospital Columbia University Medical Center - EFS New York New York
New York-Presbyterian Hospital Columbia University Medical Center - PILOT New York New York
Oregon Health & Science University Hospital - EFS Portland Oregon
UPMC Pinnacle Harrisburg Campus - EFS Wormleysburg Pennsylvania
Baylor Jack and Jane Hamilton Heart and Vascular Hospital - PILOT Dallas Texas
Houston Methodist Hospital - PILOT Houston Texas
University of Virginia Medical Center - EFS Charlottesville Virginia
Aurora Saint Luke's Medical Center - EFS Milwaukee Wisconsin
Aurora Saint Lukes Medical Center - PILOT Milwaukee Wisconsin
Monash Health - PILOT Clayton Victoria
The Alfred Hospital - PILOT Melbourne Australia
Royal Prince Alfred Hospital - PILOT Sydney Australia
Rigshospitalet - PILOT Copenhagen Denmark
Helsinki University Hospital - PILOT Helsinki Finland
Centre Hospitalier Régional Universitaire de Lille - PILOT Lille France
Clinique Pasteur - PILOT Toulouse France
Hygeia Hospital - PILOT Athens Greece
Royal Sussex County Hospital - PILOT Brighton United Kingdom
The Leeds Teaching Hospitals NHS Trust - Leeds General Infirmary - PILOT Leeds United Kingdom
Guys & St Thomas NHS Foundation Trust - St Thomas Hospital - PILOT London United Kingdom

More Medtronic Cardiovascular trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02322840 on ClinicalTrials.gov ↗ ← All trials in the UK