Efficacy Study of a Bioelectric Dressing to Treat Wounds Caused by Curettage and Electrodesiccation
| Status: | Completed |
|---|---|
| Conditions: | Hospital, Hospital |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - 80 |
| Updated: | 10/14/2017 |
| Start Date: | July 2008 |
| End Date: | October 2009 |
Efficacy of the PROCELLERA Wound Dressing in the Healing of Wounds After Curettage and Electrodesiccation of Skin Lesions
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.
silver-coated dressing, or a silver-foam dressing are effective in the treatment of wounds
resulting from curettage and electrodesiccation of skin lesions.
Inclusion Criteria:
- 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
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
- Collagen vascular disease
- Diabetes
- Venous stasis ulcers
- Participant undergoing active cancer chemotherapy
- Chronic steroid use
- Decision impairment
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