Registry for patients with aortic valve bioprostheses implanted via catheter
Official title: Registry of Aortic Valve Bioprostheses Established by Catheter
Run by French Cardiology Society · NCT01777828 · Data updated 2026-11-12
This study is tracking the long-term health of patients who have received a special type of aortic valve through a catheter to see how well they do over time.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | French Cardiology Society Academic / other |
| Locations | 1 site (Rennes) |
| Status | Recruiting |
| Started | February 2013 |
| Main results expected | February 2033 |
| Study ends | February 2034 |
| Registry record updated | February 14, 2025 |
| Trial ID | NCT01777828 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this registry are patients who have undergone transarterial or transapical aortic valve bioprosthesis implantation.
✕Probably not a fit
Patients who do not consent to participate in the registry will not benefit from the data collected.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry aims to evaluate the long-term survival of patients who have received aortic valve bioprostheses through transarterial or transapical methods. It collects data on patient outcomes over a period of up to 10 years, enhancing the information by linking it with continuous data from the French health system. The registry is mandated by French health authorities to ensure comprehensive management of patients undergoing this procedure. It includes all eligible patients who consent to participate.
Why it matters
Potential benefit: If successful, this registry could provide valuable insights into the long-term effectiveness and safety of catheter-implanted aortic valve bioprostheses, potentially improving patient outcomes.
How similar studies have gone: Previous registries have shown promise in evaluating similar interventions, indicating that this approach is supported by prior research.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Patients who have undergone transarterial or transapical aortic valve bioprosthesis implantation Exclusion Criteria: Patient has not given consent
Where it's running
-
CHU Rennes - Pontchaillou
Rennes, France Recruiting
Study contacts
- Study coordinator: Martine GILARD
- Email: francetavi@sfcardio.fr
- Phone: 33(1) 44 90 70 28
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.