What this study is
Multi-center, observational (i.e., non-interventional), open-label, real-world Registry on the Use of Kerecis Devices
What's being tested
- Kerecis Fish Skin Graft
Intervention · DEVICE
Patients already treated with a Kerecis device
Study details
- Official title
- Kerecis Real-World Fish Skin Graft Registry - "ISACOD"
- Sponsor
- Kerecis Ltd.
- Conditions
- Wounds · Pressure Ulcer · Diabetic Foot Ulcer · Venous Leg Ulcer · Surgical Wound · Soft Tissue Reinforcement
- Enrolling
- 600 people
- Starts
- 2024-08-07
- Est. completion
- 2027-06
- Record
- View on ClinicalTrials.gov ↗
Who can join
Sex ALLHealthy volunteers Not acceptedYou may qualify if
- Provided informed consent
- Has at least one target wound treated with a Kerecis device according to physician medical judgement within one calendar month prior to the registry enrollment date
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (6)
6 openMCR Health
Sarasota, Florida, United States
University Park
Sarasota, Florida, United States
Cone Health Ortho Care Greensboro
Greensboro, North Carolina, United States
Feet First Institute of Beavercreek
Beavercreek, Ohio, United States
ABC Podiatry
Columbus, Ohio, United States
South Texas Skin Cancer Center
San Antonio, Texas, United States
Study team
Sponsor
Kerecis Ltd.
Study ID KS-1000
Principal investigator
Anne Swearingen
Kerecis Ltd.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.