Menthol gloves may offer quick itch relief for eczema sufferers
NCT ID NCT07693400
First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This study tests whether wearing menthol-infused gloves and foot-covers for just five minutes a day can reduce itching in people with atopic dermatitis (eczema). Participants will use the gloves five days on, two days off for four weeks, then stop for two weeks of follow-up. The trial measures itch severity, skin appearance, quality of life, and blood markers. It also explores how menthol might work through tiny particles called exosomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- menthol-based hand and foot gloves
- What this could lead to
- If it works, this could offer a simple, drug-free way to reduce itching in eczema patients.
- What could go wrong
- This is a small Phase 2 trial with only 44 participants. The effect may be modest or no better than a sham, and some people may be allergic to menthol.
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 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 44 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2026
- Expected to finish
-
Feb 2028
An estimate. End dates often move.
- Lead sponsor
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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
-
12 to 100 years
- Sex
-
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: * 1\. Age 12 years or above. * 2\. Clinical diagnosis of atopic dermatitis based on Hanifin and Rajka criteria. * 3\. Pruritus severity defined as PP-NRS ≥ 4. * 4\. Signed the informed consent form that has been approved by the Institutional Review Board. * 5\. No changes in AD medications within four weeks before enrollment and no change in dosage during the study period. Exclusion Criteria: * 1\. Allergy to menthol. * 2\. Marked fluctuation of AD symptoms. * 3\. Secondary infection of skin lesions. * 4\. Severe peripheral vascular disease, skin lesions, or severe edema at hands/feet. * 5\. Pregnancy or breastfeeding. * 6\. Severe psychiatric conditions. * 7\. With conditions such as uremia, cirrhosis, congestive heart failure with pulmonary edema, coagulation disorders, epilepsy, alcoholism, drug abuse. * 8\. Unable to comply with the study protocol or unwilling to provide written consent. * 9\. Participation in another clinical study within the previous month. The research team may also exclude any participant who is considered unsuitable for the study.
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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
-
An Nan Hospital, China Medical University
Tainan, Taiwan, 709, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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