Efficacy Study of a Bioelectric Dressing to Treat Wounds Caused by Curettage and Electrodesiccation
Completed · Phase 2
Conditions studied: Wound Healing, Wound Infection
In brief
The purpose of this study is to determine whether a bioelectric wound dressing, a silver-coated dressing, or a silver-foam dressing are effective in the treatment of wounds resulting from curettage and electrodesiccation of skin lesions.
Key facts
- Study ID
- NCT01004055
- Run by
- Vomaris Innovations
- People needed
- 15
- Starts
- 2008-07-01
- Expected to finish
- 2009-10-01
- Last updated by the study team
- 2009-10-29
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- If female, must either be not of childbearing potential or if they are of childbearing potential must have a negative urine pregnancy test
- Wound size greater than 1x1cm
- Wound must be ≥5 cm away from all other wounds
- Wound size must not be diminished in size greater than 10% between enrollment in study and the prescreening
- 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
- Collagen vascular disease
- Diabetes
- Venous stasis ulcers
- Participant undergoing active cancer chemotherapy
- Chronic steroid use
- Decision impairment
Where it is running
- Sheftel Associates Dermatology, LLC — Oro Valley, Arizona, United States
- Sheftel Associates Dermatology, LLC — Tucson, Arizona, United States
Full record on ClinicalTrials.gov
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