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SASS 2 : Self Assembled Skin Substitute for the Autologous Treatment of Severe Burn Wounds in Acute Stage of Burn Trauma

RecruitingPhase 1, Phase 2Ages any - anyAllCHU de Quebec-Universite Laval
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In plain words

What the trial is, and whether it could suit you

This clinical trial is designed to assess the safety, effectiveness and benefits of Self Assembled Skin Substitute SASS grafts as a permanent skin replacement for the treatment of full-thickness burn wounds that require permanent coverage where the availability of donor sites is limited.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Deep second degree burns or third degree burns over 50% TBSA (Total body surface area) at time of recruitment or as determined by the surgeon; * Limited availability of donor sites for autografts; * Consent obtained by the participant or by the appropriate representative in case of inapt prospective participants or minors. Exclusion Criteria: * Skin grafting needed only on the face, hands, feet, ears or genital area; * Connective tissue diseases; * Hypersensitivity to bovine proteins; * Coagulation disorders prior being burned; * Immunodeficiency prior being burned; * Uncontrolled diabetes prior being burned; * Permanent wound coverage before SASS grafts are ready;
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What it tests

  • Self assembled skin substitute (SASS)
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Where

8 sites
Foothill Medcial Centre
Calgary, Canada
Mackenzie Health Science's Centre
Edmonton, Canada
Vancouver General Hospital
Vancouver, Canada
BC Children's Hospital Plastic Surgery Clinic
Vancouver, Canada
Winnipeg Health Science Center
Winnipeg, Canada
Hospital for Sick Children (Sickkids)
Toronto, Canada
Hôpital Sainte Justine
Montreal, Canada
CHU de Québec - Unité des grands brûlés
Québec, Canada
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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