IUCPQ
Québec, Quebec, G1V 4G5, Canada
Location status: Recruiting
Location contact
Emilie Pelletier Beaumont, MSc
CONTACT
Josep Rodes-Cabau, MD
CONTACT
Josep Rodes-Cabau, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06420830
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
Interested in participating?
Request Info18 year–80 year
All sexes
Observational
Québec, Quebec, G1V 4G5, Canada
Location status: Recruiting
Emilie Pelletier Beaumont, MSc
CONTACT
Josep Rodes-Cabau, MD
CONTACT
Josep Rodes-Cabau, MD
PRINCIPAL_INVESTIGATOR
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.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
VARC-3- defined technical success defined as:
Exclusion criteria
Patients with severe aortic stenosis undergoing transarterial TAVR with the SAPIEN 3 Ultra RESILIA valve.
Time frame: 1-3 months
Residual (peak and mean) transvalvular gradient
Time frame: 1-3 months
EOA evaluated by echocardiography imaging
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).
Time frame: 1-3 months
Paravalvular leaks evaluated by echocardiography imaging
Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.
Residual (maximal and mean) transvalvular gradient
Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.
EOA evaluated by echocardiography imaging
Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.
Bioprosthetic valve dysfunction evaluated by VARC3 criteria
Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.
Paravalvular leaks evaluated by echocardiography imaging
Time frame: yearly
Incidence rate (per 100 patient-years) of bioprosthetic valve dysfunction (stage 2 or 3)
Time frame: yearly
Incidence rate (per 100 patient-years) of bioprosthetic valve failure
Time frame: 1-, 3-5-, 6-8-, and 9-10-year follow-up.
Bioprosthetic valve failure evaluated by VARC3 criteria
Time frame: 1month and yearly up to 10-year
Individual: mortality, stroke, bleeding type 2-4, cardiac rehospitalization, heart failure rehospitalization
Time frame: 1-3 months and yearly up to 10-year
Number of patients with valve thrombosis
Time frame: 1-3 months and yearly up to 10-year
Number of patients with valve endocarditis
Contact information is provided by the study sponsor or research team.
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Other
Title Valve Performance of the SAPIEN 3 Ultra RESILIA Valve: A Prospective Registry With Central Echocardiography Analysis.
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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