MedTrace Logo

Clinical Data Collection on Perceval S Sutureless Prosthetic Aortic Valve in the Chinese Population

NCT06011148 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2024-03-06

No results posted yet for this study

Summary

The objective of the study is to evaluate the safety information on the Perceval S sutureless prosthetic heart valve after the implantation for aortic valve disease.

The study is designed as a post-market, observational, non-interventional retrospective and prospective registry.

Conditions

  • Aortic Valve Disease

Interventions

DEVICE

Perceval S sutureless heart valve

Aortic Valve Replacement with Perceval S sutureless heart valve

Sponsors & Collaborators

  • Corcym S.r.l

    lead INDUSTRY

Principal Investigators

  • Sara Gaggianesi · Corcym S.r.l

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-31
Primary Completion
2025-12-31
Completion
2025-12-31
FDA Device
Yes

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06011148 on ClinicalTrials.gov