By InvitationNot Applicable

Kerecis Real-World Fish Skin Graft Registry

United States600 participantsStarted 2024-08-07

Plain-language summary

Multi-center, observational (i.e., non-interventional), open-label, real-world Registry on the Use of Kerecis Devices

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Exclusion Criteria: * None

What they're measuring

Fish Skin Graft Device Related failure

Timeframe: 12 months

Fish Skin Graft Device related allergy

Timeframe: 12 months

Target Wound Infection

Timeframe: 12 months

Trial details

NCT IDNCT06384183

SponsorKerecis Ltd.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2026-06

View on ClinicalTrials.gov More Wounds trials