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Wound Dressing
PermeaDerm® vs. Mepilex-Ag® in Promoting Healing of Partial-thickness Burn Wounds
N/A
Waitlist Available
Led By Ludwik K Branski, MD
Research Sponsored by The University of Texas Medical Branch, Galveston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at 1 month post burn
Awards & highlights
No Placebo-Only Group
Summary
The purpose of this study is to compare the effectiveness of the wound dressings currently used at our institution for partial-thickness burn wounds: PermeaDerm® (PermeaDerm, Inc., Carlsbad, California, USA) and silver impregnated foam dressing (Mepilex Ag®, Health Care, Göteborg, Sweden)
Eligible Conditions
- Partial Thickness Burns
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at 1 month post burn
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at 1 month post burn
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Time to heal
Secondary study objectives
Cost-effectiveness
Pain assessment using Visual Analog Pain Scale (VAS) or Wong-Baker FACES pain rating scales (age dependent)
Rate of Infection
+5 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: PermeaDermActive Control1 Intervention
Participants receive PermeaDerm dressing for wound treatment until wounds have healed completely
Group II: Mepilex AgActive Control1 Intervention
Participants receive Mepilex Ag dressing for wound treatment until wounds have healed completely
Find a Location
Who is running the clinical trial?
The University of Texas Medical Branch, GalvestonLead Sponsor
254 Previous Clinical Trials
57,255 Total Patients Enrolled
Ludwik K Branski, MDPrincipal InvestigatorThe University of Texas Medical Branch, Galveston