Bee glue to the rescue? propolis ointment tested for dry skin
NCT ID NCT07618234
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether ointments made from propolis, a natural substance from honeybees, can improve dry, itchy skin in adults with atopic tendencies. Thirty participants will apply either a propolis ointment or a plain base ointment twice daily for four weeks. Researchers will measure changes in skin dryness, scaling, and itching to see if propolis offers any benefit over the base ointment alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- propolis ointment (3% ethanolic extract or 5% crude propolis)
- What this could lead to
- If it works, this could point toward a natural, over-the-counter option for managing dry, itchy skin in people with atopic tendencies.
- What could go wrong
- This is a very small, early exploratory study with only 30 participants. The results may not apply to everyone, and propolis can cause allergic reactions in some people.
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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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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30 people
The number who actually took part.
- Started
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Apr 2026
- Expected to finish
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Jun 2026
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
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18 to 60 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18-60 years * Atopic-prone dry skin or mild xerotic skin condition * Mild-to-moderate skin dryness, scaling, roughness, and mild itching * No acute inflammatory skin disease * Ability to attend follow-up visits and comply with application instructions * Signed informed consent form Exclusion Criteria: * Known allergy to propolis, honey, or bee products * Known allergy to lanolin * Acute eczema flare, infected dermatitis, psoriasis, seborrheic dermatitis, fungal infections, herpes simplex, or scabies * Pregnancy or breastfeeding * Recent use of systemic corticosteroids (within 2 weeks) * Recent use of immunosuppressants (within 4 weeks) * Recent use of biologics (within 3 months) * Recent use of topical corticosteroids (within 1 week) * Recent use of topical calcineurin inhibitors (within 1 week) * Recent phototherapy (within 2 weeks) * Severe systemic diseases not under control * Poor compliance or inability to cooperate * Use of other skin products during the study period
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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
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Manara University, Faculty of Pharmacy
Latakia, Syria
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Other studies related to the condition(s) this trial covers.
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