Status:
NOT_YET_RECRUITING
Clinical Data Collection on Perceval S Sutureless Prosthetic Aortic Valve in the Chinese Population
Lead Sponsor:
Corcym S.r.l
Conditions:
Aortic Valve Disease
Eligibility:
All Genders
Brief 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-m...
Detailed Description
In order to monitor the ongoing safety of the Perceval S as part of regulatory requirements, the study aims to retrospectively collect safety outcomes and performance data in patients with aortic valv...
Eligibility Criteria
Inclusion
- Subject who has been implanted with Perceval S sutureless aortic heart valve
- Subject (legal representative or family member) who has signed the approved informed consent or would provide verbal informed consent/ signed and dated informed consent, and available medical information
Exclusion
- 1\. Subject (legal representative or family member) who do not provide consent to the data collection
Key Trial Info
Start Date :
December 1 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT06011148
Start Date
December 1 2024
End Date
December 1 2025
Last Update
March 6 2024
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