Registry for patients with aortic valve bioprostheses implanted via catheter
Registry of Aortic Valve Bioprostheses Established by Catheter
French Cardiology Society · NCT01777828
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 |
|---|---|
| Enrollment | 5000 (estimated) |
| Sex | All |
| Sponsor | French Cardiology Society (other) |
| Locations | 1 site (Rennes) |
| Trial ID | NCT01777828 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this registry are patients who have undergone transarterial or transapical aortic valve bioprosthesis implantation.
Not a fit: Patients who do not consent to participate in the registry will not benefit from the data collected.
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 performed: Previous registries have shown promise in evaluating similar interventions, indicating that this approach is supported by prior research.
Eligibility criteria
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 this trial is running
Rennes
- CHU Rennes - Pontchaillou — Rennes, France (RECRUITING)
Study contacts
- Study coordinator: Martine GILARD
- Email: francetavi@sfcardio.fr
- Phone: 33(1) 44 90 70 28
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Transcatheter Aortic Valve Implantation