Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT07548424

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

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers who have given written informed consent
Not Eligible

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

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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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