Kerecis Fish Skin Grafts With and Without Platelet Rich Plasma (PRP)
Withdrawn before enrolling · Not applicable
Conditions studied: Non-healing Wound
In brief
This prospective, randomized pilot study compares the use of a xenograft with PRP to a xenograft alone for chronic, nonhealing wounds.
Key facts
- Study ID
- NCT05766982
- Run by
- St Elizabeth Healthcare
- People needed
- 0
- Starts
- 2024-01-30
- Expected to finish
- 2025-09-01
- Last updated by the study team
- 2024-07-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is over the age of 18 years;
- The targeted wound is deemed a chronic, nonhealing wound after six weeks of treatment; - - Patient of Dr. Eldridge, Dr. Glenn, or Dr. Worley;
- Target wound size must be between 2 cm x 2 cm x 0.1 cm deep and 10 cm x 10 cm x 5 cm deep;
- Surgical candidate for standard of care Kerecis® xenograft surgery.
You may not qualify if…
- Patient with hemoglobin values less than 6.9 g/dL drawn at least 30 days prior to the Kerecis® xenograft surgery;
- Patient with a known allergy or other sensitivity to fish material;
- Patient is currently undergoing chemotherapy or radiation therapy;
- The targeted wound is of autoimmune origin; and Non-English-speaking patients.
Where it is running
- St. Elizabeth Healthcare Edgewood — Edgewood, Kentucky, United States
Full record on ClinicalTrials.gov
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