Transcatheter Tricuspid Valve Replacement With the Medtronic Intrepid™ Transcatheter Tricuspid Valve Replacement (TTVR) System in Severe Tricuspid Regurgitation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMedtronic Cardiovascular

About this trial

This clinical trial evaluates the safety and effectiveness of the Medtronic Intrepid™ Transcatheter Tricuspid Valve Replacement (TTVR) System in symptomatic patients with severe or greater tricuspid regurgitation.

Eligibility criteria

Qualifiers

Age ≥18 years at the time of consent.

Severe symptomatic tricuspid regurgitation (TR) despite optimal medical therapy (OMT).

Local site multidisciplinary heart team experienced in tricuspid valve therapies agrees that the subject is appropriate for TTVR.

Disqualifiers

Any tricuspid device currently in place.

Anatomic contraindications.

Need for emergent or urgent surgery.

Left ventricular ejection fraction <25%.

Trial design

Treatments tested in this trial

  • Medtronic Intrepid™ Transcatheter Tricuspid Valve Replacement (TTVR) System
  • Edwards EVOQUE Tricuspid Valve Replacement (TTVR) System

Treatment groups

1,186 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators