πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-08

International Registry of Intra-arterial and Endosaccular Flow Diverters (IRF) (NCT06174727)

Outcomes of Intra-arterial and Endosaccular Flow Diverters for Treatment of Intracranial Aneurysms - International Registry of Intra-arterial and Endosaccular Flow Diverters (IRF)

🟒 Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: Montefiore Medical Center

🩺 Plain-English Summary (8th-Grade Level)

This multicenter retrospective cohort study aims to evaluate and compare the technical performance, safety, and clinical outcomes of intracranial aneurysms treated with flow diverter stents and endosaccular flow disruptors.

Who can join: Review the eligibility criteria below.

Location: University of Miami β€” Coral Gables, Florida

Age range: 18 Years

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (13 Sites)

  • University of Miami β€” Coral Gables, Florida
  • Mayo Clinic Florida β€” Jacksonville, Florida
  • Sarasota Memorial Research Institute β€” Sarasota, Florida
  • Lahey Hospital and Medical Center β€” Burlington, Massachusetts
  • Munson Medical Center β€” Traverse City, Michigan
  • Allina Health β€” Minneapolis, Minnesota
  • Robert Wood Johnson University β€” New Brunswick, New Jersey
  • University at Buffalo β€” Buffalo, New York
  • Montefiore Medical Center Department of Neurosurgery β€” The Bronx, New York
  • Geisinger Health β€” Danville, Pennsylvania
  • HCA Houston Healthcare Kingwood β€” Kingwood, Texas
  • St. Michael's Hospital β€” Toronto, Ontario
  • Toronto Western Hospital β€” Toronto, Ontario

πŸ“ž Contact the Study Coordinator

Phone: (347) 908-1889

Email: Muhammedamir.essibayi@einsteinmed.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—