Efficacy of SynEx Wound Rinse in Civilian Surrogates of Combat Injury Wounds (NCT05743283)
Efficacy of SynEx™ Wound Rinse in Civilian Surrogates of Combat Injury Wounds
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this interventional study is to compare SynEx Wound Cleanser with the current routine care (Saline) in traumatic wounds. Participants with gunshot, penetrating or burn wounds who participate will be asked to attend up to four study visits, use the assigned wound cleanser and complete brief surveys about their healing and well-being related to the wound healing.
Who can join: Review the eligibility criteria below.
Location: MedStar Washington Hospital Center — Washington D.C., District of Columbia
Age range: 18 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 (2 Sites)
- MedStar Washington Hospital Center — Washington D.C., District of Columbia
- Barnes Jewish Hospital — St Louis, Missouri
📞 Contact the Study Coordinator
Phone: (909) 447-6858
Email: sb@synedgen.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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💡 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.