Actively Recruiting
Study of a Peptide Cream's Effect on the Facial Skin Barrier Using a Side-by-Side Comparison
Led by University of Split, School of Medicine · Updated on 2026-04-23
30
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate whether a topical face cream containing the peptide Acetyl Hexapeptide-37 improves skin hydration and strengthens the skin barrier compared to a placebo cream in healthy adult participants. The study uses a split-face design, in which one side of the face is treated with the peptide cream and the other side with a placebo (a cream without the active ingredient). The main questions it aims to answer are: * Does the peptide cream improve skin hydration and reduce transepidermal water loss compared to placebo? * Does the peptide cream affect skin erythema or cause irritation? * How do participants rate the comfort and tolerability of the peptide cream? Researchers will compare the treated and placebo sides of the face to assess differences in skin barrier function and tolerability. Participants will: * Attend a baseline visit for assessment of facial skin parameters, including hydration, transepidermal water loss, and erythema * Apply the peptide cream to one side of the face and the placebo cream to the other side once daily for 4 weeks * Attend weekly follow-up visits for non-invasive skin measurements * Record any skin sensations (e.g., stinging, tightness) or adverse effects throughout the study
CONDITIONS
Official Title
Study of a Peptide Cream's Effect on the Facial Skin Barrier Using a Side-by-Side Comparison
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy volunteers who have given written informed consent
You will not qualify if you...
- Presence of active skin diseases or dermatological conditions
- Known allergy or hypersensitivity to any ingredient of the study products
- Pregnancy or breastfeeding
- Use of topical or systemic corticosteroids, immunosuppressive drugs, or antihistamines prior to or during the study
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Split School of Medicine
Split, Croatia, 21000
Actively Recruiting
Research Team
J
Josipa Bukić, MPharm
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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