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Valvosoft Outcomes Registry for Real-World Evidence
Sponsor: Cardiawave SA
Summary
The VALvosoft Outcomes Registry for Real-World Evidence (VALOR-PMCF) is a prospective, multicenter, single-arm post-market clinical follow-up (PMCF) registry designed to evaluate the long-term safety and effectiveness of the Valvosoft® non-invasive ultrasound therapy (NIUT) device in patients with severe symptomatic calcific aortic stenosis (sSAS). Valvosoft® delivers focused, high-intensity, short-duration ultrasound pulses to the aortic valve via a trans-thoracic approach, inducing non-thermal mechanical softening of calcified valve tissue. This registry will enroll up to 200 participants across approximately 20 clinical sites in Europe following CE marking. Participants will be followed from discharge through 12 months post-procedure to assess clinical outcomes, quality of life, echocardiographic parameters, and safety events in a real-world setting.
Official title: Prospective Post-Market Clinical Follow-Up Registry to Assess the Long-term Safety and Effectiveness for the Treatment of Severe Symptomatic Aortic Valve Stenosis Using Valvosoft Non-Invasive Ultrasound Therapy
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2026-05-30
Completion Date
2028-06-30
Last Updated
2026-04-09
Healthy Volunteers
No
Conditions
Interventions
Valvosoft Treatment
non-invasive ultrasound therapy for the treatment of severe symptomatic calcific AS
Locations (7)
CHU Lille Insitute Coeur Poumon
Lille, France
Hopital Bichat
Paris, France
Hopital Europeen Georges Pompidou
Paris, France
CHU Rouen Hopital Charles Nicolle
Rouen, France
Marienkrankenhaus
Hamburg, Germany
University Hospital Schleswig Holstein Campus Kiel
Kiel, Germany
RadboudUMC
Nijmegen, Netherlands