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🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2026-06-15)

Radiation Free Study

🟢 Recruiting Protocol / Phase N/A 🔬 Diagnostic & Biomarker Protocol Sponsor: Philips Clinical & Medical Affairs Global

🩺 Protocol 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)

Primary Research Facility: University of Alabama (Birmingham, Alabama)

📋 Basic Study Criteria & Logistics Checklist

0 of 3 Checked

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

📍 Primary Site Map

Site: University of Alabama — Birmingham, Alabama

📍 All Participating Trial Locations (11 Sites)

Multi-Center Trial

This protocol is enrolling participants across multiple clinical centers:

1. University of AlabamaBirmingham, Alabama
2. Beth Israel Deaconess Medical CenterBoston, Massachusetts
3. University of MassachusettsWorcester, Massachusetts
4. University of PennsylvaniaPhiladelphia, Pennsylvania
5. University of Texas Southwestern Medical CenterDallas, Texas
6. UZ GentUnited States
7. Rigshospitalet University HospitalUnited States
8. Hôpital Universitaire Pitié-SalpêtrièreUnited States
9. UMC MaastrichtUnited States
10. University Medical Center UtrechtUnited States
11. Guys & St ThomasUnited States

📄 Print Doctor Discussion Sheet

Preview and print a 1-page summary with 5 tailored questions for your physician.

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.

🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT06549348 • Last Synced: 2026-06-15
View on ClinicalTrials.gov ↗
🏛️ NIH Record 📋 Check Criteria