Vashe Wound Therapy Study

• Status: Completed
• Trial end date: 2010-11-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will evaluate the efficacy, safety, and tolerability of topical Vashe™ Wound Therapy applied to gauze dressing every 6 hours or as necessary to keep dressing moist versus 5% Mafenide Acetate applied to gauze dressing every 6 hours or as necessary to keep dressing moist for a total treatment duration of 5 days.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Maricopa Integrated Health System; Valleywise Health
• Collaborator: PuriCore, Inc.
• Treatments: Anti-Infective Agents; Mafenide

Criteria

Inclusion Criteria:

• Male or female, aged 18 years and over requiring hospitalization for burn injury

• Burn injury requiring wound excision and auto-grafting

• Less than or equal to 20% Total Body Surface Area burns

Exclusion Criteria:

• Pregnant or lactating females

• Individuals with chlorine sensitivity

• Electrical, chemical and cold injury

• Burns to the face, hands, feet and or perineum area

• Steroid therapy