πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-24

REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Ischemic Stroke (RECANOVA Registry) (NCT07599904)

🟒 Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: Medtronic Neurovascular Clinical Affairs

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

Post-Market Registry

Who can join: Review the eligibility criteria below.

Location: McLaren Flint Hospital β€” Flint, Michigan

Age range: 18 Years

πŸ§ͺ Interventions in This Study

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 (3 Sites)

  • McLaren Flint Hospital β€” Flint, Michigan
  • Buffalo General Medical Center β€” Buffalo, New York
  • University of Texas Health Science Center at Houston β€” Houston, Texas

πŸ“ž Contact the Study Coordinator

Phone: (612) 979-7251

Email: rs.recanovaregistry@medtronic.com

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†—