Evaluating a new tool for branched endovascular aortic repair
Outcome of the Semibranch in Pararenal and Thoracoabdominal Aortic Pathologies. A Retrospective, Multicentre Registry
This study is testing a new stent design for aortic repair to see if it works well and is easy to use for patients undergoing this treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital Muenster Academic / other |
| Locations | 1 site (Münster) |
| Trial ID | NCT06374355 on ClinicalTrials.gov |
What this trial studies
This observational registry aims to assess the effectiveness of the semibranch in branched endovascular aortic repair. It focuses on evaluating the patency of the semibranch and the feasibility of the technique concerning cannulation and stent-grafting. The study collects data from patients who have been treated with the semibranch stentgraft, providing insights into its performance and potential improvements in treatment outcomes.
Who should consider this trial
Good fit: Ideal candidates are patients over 18 years old who have been treated with the semibranch stentgraft.
Not a fit: Patients who have not undergone treatment with the semibranch stentgraft may not receive any benefit from this study.
Why it matters
Potential benefit: If successful, this could lead to improved treatment options for patients with aortic aneurysms.
How similar studies have performed: While this approach is relatively novel, similar studies have shown promise in evaluating new endovascular techniques.
Eligibility criteria
Show full inclusion / exclusion criteria
* Patient has been treated with the semibranch stentgraft * Patient is over 18 years old
Where this trial is running
Münster
- Muenster University Hospital — Münster, Germany (Recruiting)
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.