RecruitingNot ApplicableNCT06549348

Radiation Free Study

Sponsor

Philips Clinical & Medical Affairs Global

Enrollment

182 participants

Start Date

Jul 3, 2025

Study Type

INTERVENTIONAL

Conditions

Aortic Aneurysm

Summary

This is a prospective, randomized, unblinded, multi-center study. Sites were selected from different geographies (EU and US) with different clinical practice to ensure the results are more generalizable. Primary objective is to demonstrate that the average procedure fluoroscopy time using LumiGuide is lower compared to conventional fluoroscopy guidance in Fenestrated Endovascular Aortic Repair (FEVAR)

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Measure average procedure fluoroscopy time using LumiGuide and conventional fluoroscopy guidance for people with aortic aneurysm. The study is currently recruiting participants at 11 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONMeasure average procedure fluoroscopy time using LumiGuide and conventional fluoroscopy guidance

Fenestrated Endovascular Aortic Repair (FEVAR) procedure done with either LumiGuide or conventional fluoroscopy guidance

Locations(11)

University of Alabama

Birmingham, Alabama, United States

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

University of Massachusetts

Worcester, Massachusetts, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Texas Southwestern Medical Center

Dallas, Texas, United States

UZ Gent

Ghent, Belgium

Rigshospitalet University Hospital

Copenhagen, Denmark

Hôpital Universitaire Pitié-Salpêtrière

Paris, France

UMC Maastricht

Maastricht, Netherlands

University Medical Center Utrecht

Utrecht, Netherlands

Guys & St Thomas

London, United Kingdom

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NCT06549348

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