RecruitingNot ApplicableNCT06506942

The TRICURE EFS Study

The TRICURE EFS TRiCares Topaz Transfemoral TRICUspid Heart Valve REplacement System Early Feasibility Study


Sponsor

TRiCares

Enrollment

15 participants

Start Date

Sep 11, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Prospective, multi-center study to assess safety and performance of the TRiCares Topaz Tricuspid Valve Replacement System


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Adult patients
  • Tricuspid regurgitation grade 3 (severe) on a scale of 0 (none) to 5 (torrential)
  • Institutional Heart Team evaluates patient as being at increased operative risk

Exclusion Criteria4

  • Patient in need of emergent intervention
  • Patient who is hemodynamically unstable
  • Anatomical contraindications for implantation with study device
  • Patient who is currently participating in another clinical investigation where the primary endpoint was not reached yet

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Interventions

DEVICETranscatheter Tricuspid Valve Replacement

Replacement of the tricuspid valve through a transcatheter approach


Locations(8)

Piedmont Healthcare Inc.

Atlanta, Georgia, United States

Northwestern

Chicago, Illinois, United States

University of Michigan Hospital and Health Systems

Ann Arbor, Michigan, United States

Minneapolis Heart Institute Foundation

Minneapolis, Minnesota, United States

Columbia University Medical Center/ NewYork Presbyterian Hospital

New York, New York, United States

Montefiore

The Bronx, New York, United States

The Christ Hospital

Cincinnati, Ohio, United States

Medical University of South Carolina

Charleston, South Carolina, United States

View Full Details on ClinicalTrials.gov

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NCT06506942


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