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Retrospective Clinical Data Collection on Carbomedics OptiForm Mitral Heart Valve

Retrospective Clinical Data Collection on Carbomedics OptiForm Mitral Heart Valve

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05898230
Enrollment
400
Registered
2023-06-12
Start date
2023-11-23
Completion date
2024-12-31
Last updated
2024-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mitral Valve Disease

Brief summary

The objective of this study is to evaluate the medium- to long-term safety of the Carbomedics OptiForm Mitral Heart Valve after the implantation for mitral valve disease in the Chinese population. The study is designed as a post-market, retrospective, single arm and multicentric data collection

Detailed description

This study is conducted to evaluate the medium and long-term safety of the Carbomedics OptiForm Mitral Heart Valve after the implantation for mitral valve disease. The data will be used for regulatory purposes, to support the re-certification of the valve in the Chinese market. Valve-related SAEs such as prosthetic valve dysfunction, death, valve-related bleeding events, valve thrombosis and thromboembolic events, endocarditis and reintervention will be studied to describe the safety profile of the valve. Data of approximately 400 subjects will be collected in two clinical sites in China.

Interventions

DEVICEMitral Valve Replacement

Mitral Valve Replacement with Carbomedics OptiForm Mitral Heart Valve

Sponsors

Corcym S.r.l
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Subject who has been treated with the Carbomedics OptiForm Mitral Heart Valve. * Subject (or representative or family member) who can understand the objective of the study and is willing to provide verbal informed consent and the available medical information.

Exclusion criteria

* Subject (or legal representative or family member) who do not provide their verbal consent to the data collection, or who are unable to provide follow-up information

Design outcomes

Primary

MeasureTime frameDescription
Prosthetic Valve Dysfunctionup to 7-8 yearThe number and percentage of subjects with Prosthetic valve Dysfuntion
Mortalityup to 7-8 yearThe number and percentage of subjects died
Valve-related bleedingup to 7-8 yearThe number and percentage of subjects with Valve-related bleeding
Valve thrombosisup to 7-8 yearThe number and percentage of subjects with Valve Thrombosis
Thromboembolismup to 7-8 yearThe number and percentage of subjects with Thromboembolic events
Endocarditisup to 7-8 yearThe number and percentage of subjects with Endocarditis
Valve-Related Reinterventionup to 7-8 yearThe number and percentage of subjects underwent Valve-related reintervention

Countries

China

Contacts

Primary ContactSteven Zhang
steven.zhang@corcym.com+86 138 1023 2090
Backup ContactMichela Paroli
michela.paroli@corcym.com+39 348 8660149

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026