Clinical Trials Directory

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

TypeNameDescription
OTHERProcellera™ Antimicrobial DressingDressing indicated for partial and full-thickness wounds.
OTHERMepilex® Border LiteSelf-adherent foam dressing
DEVICEAdhesive BandageAdhesive 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.

Efficacy Study of a New Antimicrobial Wound Dressing to Treat Wounds Caused by Curettage and Electrodesiccation (NCT00816101) · Clinical Trials Directory