Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
NOT YET RECRUITING
NCT07520591

Valvosoft Outcomes Registry for Real-World Evidence

Sponsor: Cardiawave SA

View on ClinicalTrials.gov

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

Interventions

DEVICE

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