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RECRUITING
NCT02350205
PHASE1/PHASE2

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

View on ClinicalTrials.gov

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

BIOLOGICAL

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