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SASS 2 : Self Assembled Skin Substitute for the Autologous Treatment of Severe Burn Wounds in Acute Stage of Burn Trauma
Sponsor: CHU de Quebec-Universite Laval
Summary
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.
Official title: SASS 2 : Self Assembled Skin Substitute for the Autologous Treatment of Severe Burn Wounds in Acute Stage of Burn Trauma.
Key Details
Gender
All
Age Range
Any - Any
Study Type
INTERVENTIONAL
Enrollment
52
Start Date
2015-12
Completion Date
2029-01
Last Updated
2025-07-25
Healthy Volunteers
No
Conditions
Interventions
Self assembled skin substitute (SASS)
All patients in Phase B will receive Self assembled skin substitute (SASS)
Locations (7)
Foothill Medcial Centre
Calgary, Alberta, Canada
Mackenzie Health Science's Centre
Edmonton, Alberta, Canada
BC Children's Hospital Plastic Surgery Clinic
Vancouver, British Columbia, Canada
Winnipeg Health Science Center
Winnipeg, Manitoba, Canada
Hospital for Sick Children (Sickkids)
Toronto, Ontario, Canada
Hôpital Sainte Justine
Montreal, Quebec, Canada
CHU de Québec - Unité des grands brûlés
Québec, Quebec, Canada