Kerecis Real-World Fish Skin Graft Registry
NCT06384183 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 600
Last updated 2024-12-30
Summary
Multi-center, observational (i.e., non-interventional), open-label, real-world Registry on the Use of Kerecis Devices
Conditions
- Wounds
- Pressure Ulcer
- Diabetic Foot Ulcer
- Venous Leg Ulcer
- Surgical Wound
- Soft Tissue Reinforcement
Interventions
- DEVICE
-
Kerecis Fish Skin Graft
Patients already treated with a Kerecis device
Sponsors & Collaborators
-
Kerecis Ltd.
lead INDUSTRY
Principal Investigators
-
Anne Swearingen · Kerecis Ltd.
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-07
- Primary Completion
- 2026-06-30
- Completion
- 2027-06-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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