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Transcatheter Valve
Heterotopic Valve Implantation for Tricuspid Regurgitation (HOVER Trial)
Phase 3
Waitlist Available
Led By Brian P O'Neill, MD
Research Sponsored by Temple University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days, 6 months, annually to 5 years
Awards & highlights
HOVER Trial Summary
This trial is testing a new heart valve that can be implanted without open heart surgery. The goal is to see if it is safe and effective in people who are at high risk for complications from traditional surgery.
Eligible Conditions
- Tricuspid Regurgitation
HOVER Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days, 6 months, annually to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days, 6 months, annually to 5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Individual patient success
Procedural success
Secondary outcome measures
Acute kidney injury
EORTC QLQ-C30
ESAS-AM
+5 moreHOVER Trial Design
1Treatment groups
Experimental Treatment
Group I: Severe Tricuspid RegurgitationExperimental Treatment1 Intervention
This is a non-blinded (open label), non-randomized safety and feasibility study of the heterotopic implantation of the Edwards Sapien 3 valve.
Find a Location
Who is running the clinical trial?
Temple UniversityLead Sponsor
296 Previous Clinical Trials
82,789 Total Patients Enrolled
Henry Ford Health SystemLead Sponsor
300 Previous Clinical Trials
2,099,993 Total Patients Enrolled
Brian P O'Neill, MDPrincipal InvestigatorHenry Ford Hospital
Frequently Asked Questions
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