Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds

Completed · Phase 1/Phase 2

Conditions studied: Burns, Wound Healing

In brief

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.

Key facts

Study ID

NCT01061502

Run by

Vomaris Innovations

People needed

17

Starts

2009-09-01

Expected to finish

2010-11-01

Last updated by the study team

2010-12-10

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Blodgett Hospital — Grand Rapids, Michigan, United States

Full record on ClinicalTrials.gov

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