Clinical Trial

Dermocosmetic Evaluation of Propolis Ointments in Atopic-Prone Dry Skin

Study acronym: DEPRO
Active, Not Recruiting
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Summary
The goal of this clinical trial is to learn if propolis ointments work to improve dry, atopic-prone skin in adults. Propolis is a natural substance made by honeybees. It will also learn about the safety of these ointments. The main questions it aims to answer are: Does propolis ointment lower dryness, scaling, and roughness better than a base ointment with no propolis? Is there a difference between crude propolis and ethanolic extract of propolis (EEP)? Researchers will compare three ointments to see if they improve skin condition: A propolis ointment made with 3% ethanolic extract A propolis ointment made with 5% crude propolis A base ointment with no propolis (look-alike) Participants will: Apply the ointment to dry skin areas twice a day for 4 weeks Visit the clinic 4 times: for screening, at the start, at week 2, and at week 4 Have their skin checked by a researcher using a standard dryness score Answer questions about skin comfort, itching, and satisfaction Have a patch test before starting to check for allergy to propolis
Trial Details
NCT Number NCT07618234
Lead Sponsor Manara University
Conditions Dry Skin, Atopic Dermatitis, Xerosis Due to Atopic Dermatitis
Enrollment 30 participants
Start Date 2026-04-15
Primary Completion 2026-05-24 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2026-06-01