Cold plasma zaps away Kids' skin lesions in new trial
NCT ID NCT05937672
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a cold atmospheric plasma device on children aged 4-21 with warts or molluscum lesions. The device uses ionized gas to treat the lesions without heat. The trial was terminated early, so we don't have full results on how well it worked or its safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cold atmospheric plasma device
- What this could lead to
- If successful, this could provide a non-invasive, painless treatment option for common skin lesions in children.
- What could go wrong
- The trial was terminated early, so we don't have clear evidence it works. It was also a small study with only 60 participants.
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
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
60 people
The number who actually took part.
- Started
-
Sep 2023
- Finished
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Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
4 to 21 years
- Sex
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Anyone
- Healthy volunteers
-
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: * All patients from 4-21 years old with at least 1 lesion of vercurra or molluscum. * Willingness of the participant and their guardian to provide consent when applicable. Exclusion Criteria: * Unwillingness to participate in the study * Received any treatment on the lesion in the past month determined by review of their medical record * Immunodeficiency determined by review of their medical record. * Adverse response to prior treatments determined by review of medical record. * Signs of self-resolution determined by study team members. * Conditions that lead to excessive scarring determined by study team members. * Face and genital lesions determined by study team members.
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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.
Contacts and locations
Locations
-
Medical University of South Carolina
Charleston, South Carolina, 29425, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.