Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds (NCT01061502) | Clinical Trial Compass
CompletedPhase 1/2
Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds
United States17 participantsStarted 2009-09
Plain-language summary
The purpose of this study is to determine whether the use of a bioelectric wound dressing is effective in the healing of skin graft donor site wounds.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion Criteria:
* Wounds resulting from skin graft
* Split thickness wound
* Wound size greater than 2x2 cm
* Wounds must be ≥5 cm away from all other wounds
* Participant agrees to participate in follow-up evaluation
* Participant must be able to read and understand informed consent, and sign the informed consent
Exclusion Criteria:
* Concurrent participation in another clinical trial that involves an investigational drug or device that would interfere with this study
* Participant is to receive another topical antimicrobial agent other than the study dressing
* Participant with sensitivity or adverse reactions to silver or zinc
* Pregnancy or nursing an infant or child
* Immunosuppression
* Active or systemic infection
* Peripheral vascular occlusive disease
* Collagen vascular disease
* Connective tissue disease
* Participant undergoing active cancer chemotherapy
* Chronic steroid use
* Decision impairment