Novel Strategies for Reducing Burn Scar Itch (NCT06801626)

🧪 Interventions in This Study

• Famotidine and 4% topical cromolyn sodium (COMBINATION_PRODUCT)

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

📍 All Participating Trial Locations (1 Sites)

• University of Texas Medical Branch, Galveston — Galveston, Texas

📞 Contact the Study Coordinator

Phone: (409) 266-2678

Email: listurm@utmb.edu

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.

More studies in Burn Scar

• Microneedling for Burn Hypertrophic Scars — Montreal,
• CO2 Laser Revision for Burn Related Donor Site Scars — Washington D.C., District of Columbia
• Post-Operative Use of FS2 to Mitigate Scarring in Burn Patients — Edmonton, Alberta
• The Role of Fractional Vascular Laser Therapy in the Management of Burn Scars — Winnipeg, Manitoba
• The Role of Pulsed Dye Laser Therapy in the Management of Burn Scars — Winnipeg, Manitoba

Explore by condition: All Burn Scar 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.