About this trial
The study will examine the effectiveness of a decellularized dermal matrix (i.e., DermGEN™) in improving wound healing, quality of life and associated costs of treatment of DFUs in First Nations people living in the Northwestern Ontario Communities. First Nations people with active diabetic foot (DFU) ulcer attending a wound care clinic located at the Rainy River district office. An interventional, two-arm, randomized, prospective study of (1) standard of care (control) vs. (2) DermGEN™ - a decellularized dermal matrix (treatment) will be used in the treatment and management of DFU. Patients will be randomized to each arm (n=60 per arm) based on power calculations using data from our Pilot study.
Eligibility criteria
Qualifiers
Participant and social support (e.g., family, caregiver) ready and willing to participate and comply with follow-up regime
Participant willing to be involved in self-care (e.g., keep dressing dry at home) required during treatment
Participant willing to wear Total Contact Cast (TCC) for wound off-loading during treatment
Participant or legal representative has read and signed the informed consent form
Disqualifiers
The individual has any condition that seriously compromises their capacity to provide consent and answers questions related to this study.
Untreated infection of soft tissue or bone and/or autoimmune connective tissue disorders
Ulcer is over Charcot deformity (joints deformity of foot and ankle common in people with diabetes)
Body mass index ≥50 kg/m2
Trial design
Treatments tested in this trial
- Standard of Care
- DermGEN™
Treatment groups
Sponsors and collaborators
DeCell Technologies Inc.
Lead sponsor
Dalhousie University
Sponsor institution
Canadian Institutes of Health Research (CIHR)
Collaborator
Dalhousie University
Collaborator
Lakehead University
Collaborator