Observational registry for Iliac E-liac Branch Device in treating aortoiliac aneurysms
CAMpania PugliA bRanch Iliaco
This study is looking at how well the Iliac E-liac Branch Device works for treating aortoiliac aneurysms in patients over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Sex | All |
| Sponsor | Federico II University Academic / other |
| Locations | 2 sites (Bari, BA and 1 other locations) |
| Trial ID | NCT06946381 on ClinicalTrials.gov |
What this trial studies
This observational registry aims to evaluate the medium and long-term performance of the Iliac E-liac Branch Device from Artivion in treating aortoiliac aneurysms. It involves a multicentric approach, collecting data from consecutive patients who meet specific inclusion criteria. The study focuses on real-world outcomes and effectiveness of the device in a clinical setting, providing valuable insights into its use. Patients treated with the E-liac stent-graft system, either alone or in combination with other devices, will be included in the registry.
Who should consider this trial
Good fit: Ideal candidates are patients with an aortoiliac or aortic aneurysm of surgical interest treated with the E-liac stent-graft system.
Not a fit: Patients who refuse to participate or are treated with devices other than the E-liac stent-graft system may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance treatment options and outcomes for patients with aortoiliac aneurysms.
How similar studies have performed: Other studies have shown success with similar endovascular approaches, suggesting potential for positive outcomes in this registry.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * An aortoiliac or aortic aneurysm of surgical interest based on the most recent local guidelines treated with the E-liac stent-graft system, alone or in combination with other devices Exclusion Criteria: * Patient's refusal to be enrolled in the registry * Patient treated with devices not including the E-liac stent-graft system
Where this trial is running
Bari, BA and 1 other locations
- Azienda ospedaliero-universitaria consorziale policlinico di Bari — Bari, Ba, Italy (Recruiting)
- Azienda Ospedaliera Universitaria Federico II — Naples, Italy (Recruiting)
Study contacts
- Study coordinator: Umberto Marcello UM Bracale, PhD, Prof.
- Email: chirurgiavascolarefedericoii@gmail.com
- Phone: 081 746 2629
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.