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Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis
NCT06218875 · View on ClinicalTrials.gov ↗
Study Summary
A prospective, observational post-market registry collecting outcomes through a 10-year post procedure follow-up for patients treated with the GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) or the GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device) as a part of routine clinical practice.
Conditions Studied
Study Locations (20)
California
- University of California - Irvine — Irvine
- University of Southern California — Los Angeles
- University of Southern California — Los Angeles
- Stanford University School of Medicine — Palo Alto
- Stanford University School of Medicine — Stanford
Georgia
- VA Medical Center- Atlanta — Atlanta
- Emory Saint Joseph's Hospital — Atlanta
- Augusta University Medical Center — Augusta
- Atlanta VA Medical Center — Decatur
Florida
- Mount Sinai Vascular Institute — Miami Beach
- University of South Florida — Tampa
- University of South Florida — Tampa
Illinois
- University of Chicago Hospital — Chicago
- Endeavor Health — Evanston
Arkansas
- Central Arkansas Veteran's Healthcare System — Little Rock
Indiana
- St. Vincent Medical Group, Inc. — Indianapolis
Kentucky
- University of Louisville — Louisville
Louisiana
- Our Lady of the Lake Regional Medical Center — Baton Rouge
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,000 participants |
| Start Date | 2024-05-07 |
| Est. Completion | 2042-09-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06218875
The ClinicalTrials.gov registry entry for NCT06218875 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is W.L.Gore & Associates, which has 117 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with AAA - Abdominal Aortic Aneurysm appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06218875 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Georgia, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06218875 about?
NCT06218875 is a clinical study titled "Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis". A prospective, observational post-market registry collecting outcomes through a 10-year post procedure follow-up for patients treated with the GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) or the GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device) as a part of routine clinical pr...
What is the current status of trial NCT06218875?
This trial is currently recruiting. The enrollment target is 2,000 participants. The study started on 2024-05-07. Estimated completion is 2042-09-30.
What conditions does trial NCT06218875 study?
This clinical trial studies the following conditions: AAA - Abdominal Aortic Aneurysm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
Who is sponsoring clinical trial NCT06218875?
This trial is sponsored by W.L.Gore & Associates, which has 117 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06218875 being conducted?
This trial has 20 study locations across Arkansas, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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