🏛️ Verified NIH Record • Updated 2026-08-21
The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck Bifurcating Intracranial Aneurysms (IAs). (NCT02998229)
Artisse™ Intrasaccular Device IDE
🟢 Recruiting Observational / Diagnostic ⚙️ Medical Device Protocol Sponsor: Medtronic Neurovascular Clinical Affairs
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to assess the safety and effectiveness of the Artisse™ Intrasaccular Device in the treatment of unruptured and ruptured wide-neck bifurcating intracranial aneurysms.
Who can join: Review the eligibility criteria below.
Location: USC - Keck School of Medicine — Los Angeles, California
Age range: 18 Years to 75 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (25 Sites)
- USC - Keck School of Medicine — Los Angeles, California
- Swedish Medical Center — Englewood, Colorado
- Yale New Haven Hospital — New Haven, Connecticut
- Baptist Medical Center Jacksonville — Jacksonville, Florida
- Tampa General Hospital — Tampa, Florida
- University of Chicago — Chicago, Illinois
- Advocate Lutheran General Hospital — Park Ridge, Illinois
- Ascension Saint Vincent Hospital - Indianapolis — Indianapolis, Indiana
- University of Iowa Hospitals and Clinics — Iowa City, Iowa
- Massachusetts General Hospital — Boston, Massachusetts
- Cooper University Health — Camden, New Jersey
- Albany Medical Center — Albany, New York
- Buffalo General Medical Center — Buffalo, New York
- The Mount Sinai Hospital — New York, New York
- Stony Brook University Hospital — Stony Brook, New York
- Novant Health Brain and Spine Surgery — Charlotte, North Carolina
- Cleveland Clinic Foundation — Cleveland, Ohio
- Oklahoma University Medical Center — Oklahoma City, Oklahoma
- Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania
- Thomas Jefferson University Hospital — Philadelphia, Pennsylvania
- UPMC Presbyterian — Pittsburgh, Pennsylvania
- Prisma Health — Greenville, South Carolina
- Semmes Murphy Clinic — Memphis, Tennessee
- University of Utah Hospital — Salt Lake City, Utah
- West Virginia University — Morgantown, West Virginia
📞 Contact the Study Coordinator
Phone: (949) 837-3700
Email: rs.nvclinicalartisse@medtronic.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 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 § 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.
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Explore by condition: All Intracranial Aneurysm clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.