Randomized Controlled Trial to Investigate Clinical Outcomes and Associated Costs When PermeaDerm is Used as Temporary Dressing for Surgical Wounds (NCT06750809)
A Prospective Post-Market Multicenter Randomized Controlled Clinical Study to Investigate Clinical Outcomes and Associated Costs When PermeaDerm is Used as Temporary Dressing for the Management of Surgical Wounds
🩺 Plain-English Summary (8th-Grade Level)
The goal of this study is to compare the cost and clinical outcomes for two temporary dressings (Allograft and PermeaDerm) used in patients that need a skin graft to heal their wound. The researchers will review cost and other treatment results including how well both temporary dressings attach to the skin, how prepared the wound bed is to receive a skin graft, how long it takes for the skin to be ready to receive a skin graft, how well the skin graft takes and any complications. Patients will first have the temporary dressing applied to their wound, then a few days later, a skin graft will be performed. Patients will have photos of their wounds taken throughout the study including at all the clinic check-ups with the last check-up occurring about 8 weeks after treatment.
Who can join: Review the eligibility criteria below.
Location: Valleywise Health — Phoenix, Arizona
🧪 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 (13 Sites)
- Valleywise Health — Phoenix, Arizona
- Medstar Washington Hospital Center — Washington D.C., District of Columbia
- Grady Memorial — Atlanta, Georgia
- Univ of Iowa — Iowa City, Iowa
- University of Kansas — Kansas City, Kansas
- Univ of Louisville Burn Center — Louisville, Kentucky
- University Medical Center — New Orleans, Louisiana
- University of Rochester — Rochester, New York
- Atrium Health Wake Forest Baptist — Winston-Salem, North Carolina
- Akron Children's Hospital — Akron, Ohio
- Ohio State University — Columbus, Ohio
- Regional One Firefighter's Burn Center — Memphis, Tennessee
- Virginia Commonwealth University — Richmond, Virginia
💰 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 Surgical Wound
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- Regenn® Therapy System Safety Study — Kansas City, Kansas
- Use of Fish Skin Graft (FSG) to Improve Wound Healing and Expedite Discharge at a County Safety-net Hospital — Houston, Texas
- Early Versus Delayed Bathing of Orthopaedic Surgical Wounds — New York, New York
- A Prospective Study Using SupraSDRM® in Promoting Healing and Reducing the Time to Grafting of Full-thickness Wounds — Fort Sam Houston, Texas
Explore by condition: All Surgical Wound clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.