Optimal Stent Duration After Ureteroscopy (NCT06045962)

🧪 Interventions in This Study

• Ureteral stent (DEVICE)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (11 Sites)

• Mayo Clinic Arizona — Phoenix, Arizona
• University of Arizona — Tucson, Arizona
• University of California San Diego — San Diego, California
• Johns Hopkins University — Baltimore, Maryland
• Mayo Clinic Minnesota — Rochester, Minnesota
• Montefiore Medical Center — The Bronx, New York
• University of North Carolina — Chapel Hill, North Carolina
• Cleveland Clinic — Cleveland, Ohio
• Vanderbilt University — Nashville, Tennessee
• University of British Columbia — Vancouver, British Columbia
• University of Montreal — Montreal, Quebec

📞 Contact the Study Coordinator

Phone: (800) 664-4580

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.

Explore by condition: All Ureteral Stent clinical trials

💡 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.