Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns
Recruiting now · Phase 2
Conditions studied: Burns
In brief
To compare MW-III to Silvadene® Cream 1% (Silver Sulfadiazine) with respect to "time to healing" (≥95% re-epithelialization) of a partial thickness target thermal burn.
Key facts
- Study ID
- NCT01297400
- Run by
- Skingenix, Inc.
- People needed
- 60
- Starts
- 2022-03-11
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-03-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults, 18 years of age or older on the day of signing the informed consent.
- Thermal Burns not exceeding a total body surface area (TBSA) OF 25%, with at least one partial thickness burn of 0.5% TBSA or greater. If full thickness burn(s) are present at screening, the total full thickness burn area shall not exceed 10% TBSA. Note: TBSA excludes areas of superficial (first degree) burns.
- Able and willing to give informed consent and comply with study procedures.
You may not qualify if…
- Any burn that at screening is:
- infected.
- circumferential or deemed, in the judgment of the investigator, at high risk for developing compartment syndrome.
- partial thickness that is likely, in the judgment of the Investigator, to require grafting within 72 hours, or other non-protocol intervention.
- Severe inhalation injury or other significant non-burn trauma.
Where it is running
- Valleywise Health Medical Center — Phoenix, Arizona, United States (enrolling)
- University of CA Davis Medical Center — Sacramento, California, United States (enrolling)
- MedStar Washington Hospital Center — Washington D.C., District of Columbia, United States (enrolling)
- University of Iowa Health Care — Iowa City, Iowa, United States (enrolling)
- Proactive CR Mexico SA de CV — Irapuato, Mexico (enrolling)
- SMIQ S de R. L de CV — Querétaro City, Mexico (enrolling)
Full record on ClinicalTrials.gov
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