New burn cream aims to speed healing in phase 2 trial
NCT ID NCT01297400
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new cream called MW-III on partial-thickness thermal burns (like from fire or hot liquids). It compares MW-III to a standard burn cream, Silvadene, to see which helps burns heal faster. About 60 adults with burns covering up to 25% of their body will take part. The main goal is to measure time to 95% healing.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2022
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adults, 18 years of age or older on the day of signing the informed consent. 2. 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. 3. Able and willing to give informed consent and comply with study procedures. Exclusion Criteria: 1. Any burn that at screening is: 1. infected. 2. circumferential or deemed, in the judgment of the investigator, at high risk for developing compartment syndrome. 3. partial thickness that is likely, in the judgment of the Investigator, to require grafting within 72 hours, or other non-protocol intervention. 2. Severe inhalation injury or other significant non-burn trauma.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
6 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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MedStar Washington Hospital Center
RECRUITINGWashington D.C., District of Columbia, 20010, United States
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Proactive CR Mexico SA de CV
RECRUITINGIrapuato, Mexico
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SMIQ S de R. L de CV
RECRUITINGQuerétaro City, Mexico
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University of CA Davis Medical Center
RECRUITINGSacramento, California, 95817, United States
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University of Iowa Health Care
RECRUITINGIowa City, Iowa, 52242, United States
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Valleywise Health Medical Center
RECRUITINGPhoenix, Arizona, 85008, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a dissolvable dressing get burn patients to skin grafts faster?
- Could a special dressing make skin grafts unnecessary for burns?
- Can tiny skin grafts heal wounds without leaving a second scar?
- Lab-Grown skin could transform burn healing