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NCT Number: NCT06420830

Valve Performance of the SAPIEN 3 Ultra RESILIA Valve: A Prospective Registry With Central Echocardiography Analysis.

The issue of valve durability has become one of the most important aspects in the TAVR field in recent years since transcatheter aortic valve replacement has been progressively applied to younger patients with a low co-morbidity burden. The SAPIEN 3 Ultra RESILIA valve represents the last generation of the SAPIEN valve system and includes several important iterations (newer leaflet calcium-blocking technology targeting calcium-attracting free aldehydes, dry tissue storage, newer skirt textile design) that should translate into a favorable impact on valve durability at mid- to long- term follow-up

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Prospective observational registry including patients with severe aortic stenosis undergoing TAVR with the SAPIEN 3 Ultra RESILIA valve. All patients who will survive the procedure will undergo a clinical and echocardiographic follow-up at 1-3 months (± 15 days), at 1-year (±30 days), 3-5 year (±30 days), 6-8 year (±30 days) and 9-10 year (±30 days) after valve implantation. Transthoracic echocardiography (TTE) exams (baseline, 1-3-month, 1 year, 3-5 years, 6-8 years, and 9-10 years post-procedure) will be evaluated in a Centralized Echocardiographic Core Lab at the Quebec Heart and Lung Institute. The measurements obtained in the Core Lab regarding transvalvular gradient, EOA, PPM and PVL at 1-3 months will determine the primary outcome of the study.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inclusion criteria - Patients with severe aortic stenosis undergoing transarterial TAVR with the SAPIEN 3 Ultra RESILIA valve.
  • Successful valve implantation of the SAPIEN 3 Ultra RESILIA valve.

VARC-3- defined technical success defined as:

  • Freedom from mortality
  • Successful access, delivery of the device, and retrieval of the delivery system
  • Correct positioning of a single prosthetic heart valve into the proper anatomical location
  • Freedom from surgery or intervention related to the device (excluding permanent pacemaker) or to a major vascular or access related, or cardiac structural complication - Absence of severe procedural or in-hospital complications (VARC-3 definitions): mortality, stroke, bleeding type 2-4, myocardial infarction, need for a second valve, valve embolization, coronary obstruction, annular rupture.

Exclusion criteria

  • Age >80 years
  • Severe pulmonary disease (FEV1 <50% predicted or need for home oxygen)
  • Severe renal dysfunction (eGFR <30 ml/min/1.73m2)
  • Frailty (Clinical Frailty Scale > 4)
  • Severe coronary disease (SYNTAX score >32)
  • Left ventricular ejection fraction ≤30%
  • Moderate-to-severe mitral regurgitation
  • Severe tricuspid regurgitation
  • Pulmonary systolic pressure >60 mmHg
  • STS-PROM >5%
  • Any disease leading to a life expectancy <5 years

Treatment and study plan

SAPIEN 3 Ultra RESILIA Valve

Procedure

Patients with severe aortic stenosis undergoing transarterial TAVR with the SAPIEN 3 Ultra RESILIA valve.

Primary outcomes

  1. Transvalvular gradient

    Time frame: 1-3 months

    Residual (peak and mean) transvalvular gradient

  2. Effective orifice area (EOA)

    Time frame: 1-3 months

    EOA evaluated by echocardiography imaging

  3. Prosthesis-patient mismatch

    Time frame: 1-3 months

    Moderate or severe prothesis-patient mismatch (defines as an index aortic valve area 0.85-0.66 cm2/m2 (moderate), ≤0.65 cm2/m2 (severe) for patient with BMI ˂30km/m2 and 0.70-0.56 cm2/m2 (moderate), ≤0.55 cm2/m2 (severe) for patient with BMI ≥30km/m2 and/or moderate-severe aortic regurgitation (AR) (VARC-3 definition).

  4. Paravalvular leaks

    Time frame: 1-3 months

    Paravalvular leaks evaluated by echocardiography imaging

Secondary outcomes

  1. Transvalvular gradient

    Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.

    Residual (maximal and mean) transvalvular gradient

  2. Effective orifice area (EOA)

    Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.

    EOA evaluated by echocardiography imaging

  3. Bioprosthetic valve dysfunction

    Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.

    Bioprosthetic valve dysfunction evaluated by VARC3 criteria

  4. Paravalvular leaks

    Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.

    Paravalvular leaks evaluated by echocardiography imaging

  5. Bioprosthetic valve dysfunction

    Time frame: yearly

    Incidence rate (per 100 patient-years) of bioprosthetic valve dysfunction (stage 2 or 3)

  6. Bioprosthetic valve failure

    Time frame: yearly

    Incidence rate (per 100 patient-years) of bioprosthetic valve failure

  7. Bioprosthetic valve failure

    Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.

    Bioprosthetic valve failure evaluated by VARC3 criteria

  8. Clinical events

    Time frame: 1month and yearly up to 10-year

    Individual: mortality, stroke, bleeding type 2-4, cardiac rehospitalization, heart failure rehospitalization

  9. Valve thrombosis

    Time frame: 1-3 months and yearly up to 10-year

    Number of patients with valve thrombosis

  10. Valve endocarditis

    Time frame: 1-3 months and yearly up to 10-year

    Number of patients with valve endocarditis

Study contacts

Contact information is provided by the study sponsor or research team.

Emilie Pelletier beaumont, MSc

CONTACT

[email protected]

418-656-8711 ext. 3929

Josep Rodés-Cabau, MD

CONTACT

[email protected]

4186568711

Sponsors and collaborators

Lead sponsor

Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

Other

Registry information

Official study title

Title Valve Performance of the SAPIEN 3 Ultra RESILIA Valve: A Prospective Registry With Central Echocardiography Analysis.

Important dates

Study start
2024
Primary completion
2026
Study completion
2034
First posted
May 20, 2024
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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