MedTrace Logo

Global Iliac Branch Study

NCT05607277 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 297

Last updated 2024-04-19

No results posted yet for this study

Summary

This project seeks to determine if certain anatomic factors, specifically tortuous and non-conformable iliac arteries, may predict device complications, including seal zone failure, type III endoleak, and occlusion. Approximately 400 subjects from 5 academic centers across the United States, Europe, and Asia will be included in this study. Various markers of pre- and post-treatment iliac anatomy will be measured using CT imaging, and clinical events will be reported by academic centers. The relationship of imaging data to patient demographics will then be assessed alongside anatomic and demographic predictors of non-conformability.

Conditions

  • Abdominal Aortic Aneurysm
  • Iliac Aneurysm

Interventions

PROCEDURE

Endovascular Repair of abdominal aortic aneurysms

Femoral artery access

Sponsors & Collaborators

  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • Jon Matsumura, MD · University of Wisconsin, Madison

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2020-12-31
Completion
2021-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05607277 on ClinicalTrials.gov