A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE) | MicrobiomeTrials← Back to trialsNCT06568627
A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE)
RecruitingPHASE3INTERVENTIONAL
Trial Details
Start: 2025-06-01Est. Completion: 2026-12
Enrollment target: 216 participants Locations- Synergy Wound 360, PLLC, Phoenix, Arizona, United States
- Limb Preservation Platform, Inc, Fresno, California, United States
- Angel City Research,Inc, Los Angeles, California, United States
- North Park Podiatry, San Diego, California, United States
- Center for Clinical Research INC, San Francisco, California, United States
- ILD Research Center, Vista, California, United States
- MedStar Washington Hospital Center, Washington D.C., District of Columbia, United States
- University of Miami, Miami, Florida, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Boston Medical Center, Boston, Massachusetts, United States
- Rutgers New Jersey Medical Center, Newark, New Jersey, United States
- Northwell Health Comprehensive Wound Healing Center, Lake Success, New York, United States
- NYU Langone Health Long Island - Research & Academic Center, Mineola, New York, United States
- Mount Sinai West, New York, New York, United States
- Cutting Edge Research LLC.,, Circleville, Ohio, United States
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