TRISCEND II Pivotal Trial
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ClinicalTrials.gov Identifier: NCT04482062 |
Recruitment Status :
Recruiting
First Posted : July 22, 2020
Last Update Posted : March 6, 2023
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Tricuspid Valve Regurgitation Tricuspid Valve Insufficiency Tricuspid Valve Disease Heart Valve Diseases Cardiovascular Diseases Heart Failure | Device: Edwards EVOQUE System Drug: Optimal Medical Therapy | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 820 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Edwards EVOQUE Transcatheter Tricuspid Valve Replacement: Pivotal Clinical Investigation of Safety and Clinical Efficacy Using a Novel Device |
Actual Study Start Date : | April 9, 2021 |
Estimated Primary Completion Date : | June 2024 |
Estimated Study Completion Date : | June 2028 |
Arm | Intervention/treatment |
---|---|
Experimental: Edwards EVOQUE System & OMT
Transcatheter tricuspid valve replacement with the Edwards EVOQUE System in conjunction with optimal medical therapy (OMT) in patients with tricuspid regurgitation
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Device: Edwards EVOQUE System
Transcatheter tricuspid valve replacement with the Edwards EVOQUE System in conjunction with OMT
Other Name: Transcatheter tricuspid valve replacement |
Active Comparator: Optimal Medical Therapy (OMT)
Optimal medical therapy (OMT) alone in patients with tricuspid regurgitation
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Drug: Optimal Medical Therapy
Optimal Medical Therapy |
Experimental: Single-Arm Registry
Transcatheter tricuspid valve replacement with the Edwards EVOQUE System in conjunction with optimal medical therapy (OMT) in patients with tricuspid regurgitation who are not eligible for randomization
|
Device: Edwards EVOQUE System
Transcatheter tricuspid valve replacement with the Edwards EVOQUE System in conjunction with OMT
Other Name: Transcatheter tricuspid valve replacement |
- TR Grade reduction and composite endpoint including: Kansas City Cardiomyopathy Questionnaire (KCCQ) improvement, New York Heart Association (NYHA) functional class improvement, and 6-minute walk test distance improvement [ Time Frame: 6 months ]Comparison of number of participants with reduction in TR and composite endpoint event improvement between experimental and active comparator arms
- Rate of Major Adverse Events (MAE) [ Time Frame: 30 days ]Rate of Major Adverse Events (MAE) in experimental arm
- Composite endpoint including all-cause mortality, RVAD implantation or heart transplant, tricuspid valve intervention, heart failure hospitalizations, KCCQ improvement, NYHA functional class improvement, and 6-minute walk distance improvement [ Time Frame: 1 year ]Comparison of number of participants with composite endpoint events between experimental and active comparator arms
- Composite endpoint including reduction in TR grade, change in QOL from baseline, death and heart failure hospitalization, all-cause hospitalization, all-cause mortality, and change in right ventricular end diastolic volume index [ Time Frame: 1 year ]Hierarchical comparison of number of participants with composite endpoint events between experimental and active comparator arms

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Symptomatic tricuspid regurgitation (TR) despite medical therapy
- TR graded as severe or greater
- Appropriate for transcatheter tricuspid valve replacement per the local heart team
Exclusion Criteria:
- Tricuspid valve anatomic contraindications
- Need for emergent or urgent surgery or any planned cardiac surgery within the next 12 months
- Hemodynamic instability
- Refractory heart failure requiring advanced intervention
- Currently participating in another investigational study

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04482062
Contact: TMTT Clinical | 949-250-2500 or 800-424-3278 | TMTT_Clinical@Edwards.com |

Principal Investigator: | Rebecca Hahn, MD | Columbia University | |
Principal Investigator: | Susheel Kodali, MD | Columbia University | |
Principal Investigator: | Philipp Lurz, MD | Herzzentrum Leipzig GmbH | |
Principal Investigator: | Vinod Thourani, MD | Piedmont Heart Institute |
Responsible Party: | Edwards Lifesciences |
ClinicalTrials.gov Identifier: | NCT04482062 |
Other Study ID Numbers: |
2020-05 |
First Posted: | July 22, 2020 Key Record Dates |
Last Update Posted: | March 6, 2023 |
Last Verified: | March 2023 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | Yes |
Device Product Not Approved or Cleared by U.S. FDA: | Yes |
Cardiovascular Diseases Heart Valve Diseases Tricuspid Valve Insufficiency Heart Diseases |