Clinical Trials Directory

Trials / Completed

CompletedNCT01004055

Efficacy Study of a Bioelectric Dressing to Treat Wounds Caused by Curettage and Electrodesiccation

Efficacy of the PROCELLERA Wound Dressing in the Healing of Wounds After Curettage and Electrodesiccation of Skin Lesions

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Vomaris Innovations · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEProcellera™ Antimicrobial Wound DressingDressing indicated for partial and full-thickness wounds. Dressing changes every 2-3 days, more frequently if needed
DRUGACTICOAT™ Antimicrobial Barrier DressingDressing changes every 2-3 days, more frequently if needed
DRUGMepilex® Ag Silver Foam DressingDressing changes every 2-3 days, more frequently if needed

Timeline

Start date
2008-07-01
Primary completion
2009-08-01
Completion
2009-10-01
First posted
2009-10-29
Last updated
2009-10-29

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01004055. Inclusion in this directory is not an endorsement.