Trials / Completed
CompletedNCT00816101
Efficacy Study of a New Antimicrobial Wound Dressing to Treat Wounds Caused by Curettage and Electrodesiccation
Efficacy of the PROCELLERA™ Wound Dressing in the Healing of Wounds After a Curettage and Electrodesiccation of Skin Lesions
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Vomaris Innovations · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this pilot clinical study is to compare healing rates, pain levels, and incidence of wound complications including infection with the use of a moist PROCELLERA™ Antimicrobial Wound Dressing when compared to a standard dressing, Mepilex® Border Lite, following curettage and electrodesiccation of skin lesions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Procellera™ Antimicrobial Dressing | Dressing indicated for partial and full-thickness wounds. |
| OTHER | Mepilex® Border Lite | Self-adherent foam dressing |
| DEVICE | Adhesive Bandage | Adhesive bandage |
Timeline
- Start date
- 2008-03-01
- Primary completion
- 2008-09-01
- Completion
- 2008-10-01
- First posted
- 2008-12-31
- Last updated
- 2011-03-09
- Results posted
- 2011-03-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00816101. Inclusion in this directory is not an endorsement.