Comparison of Skin Condition After Hyaluronic Acid Application on Dry vs. Moist Skin
Comparison of Different Methods of Hyaluronic Acid Application on Skin Parameters
1 other identifier
interventional
23
1 country
1
Brief Summary
This study aims to compare the effects of two different methods of applying hyaluronic acid (HA) on skin parameters in healthy individuals. HA is a widely used ingredient in skincare products due to its hydrating properties. However, it is unclear whether applying HA to dry or pre-moistened skin provides better results in terms of skin hydration and texture. In this non-invasive, interventional trial, 23 healthy volunteers aged 18 to 50 will be randomly assigned to two groups. One group will apply HA to dry skin, while the other will apply HA to moistened skin. Skin parameters will be measured before and after the intervention to assess hydration, transepidermal water loss, and overall skin condition. The aim is to determine the optimal method of HA application that maximizes its effectiveness in improving skin quality. Participants may benefit from improved skin hydration and increased awareness of the best application method for their skin type. No significant risks are expected from participation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 9, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 9, 2025
CompletedFirst Submitted
Initial submission to the registry
July 11, 2025
CompletedFirst Posted
Study publicly available on registry
July 22, 2025
CompletedJuly 22, 2025
June 1, 2025
21 days
July 11, 2025
July 11, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Change in skin hydration level
Skin hydration will be measured at four time points using a corneometer or comparable non-invasive skin analysis device. Measurements will be taken before the intervention (baseline) and at the end of each week to assess cumulative and comparative effects of hyaluronic acid application.
Baseline, Week 1, Week 2, Week 3
Study Arms (2)
Dry Skin Application
EXPERIMENTALParticipants in this group applied hyaluronic acid topically to clean, dry skin. The aim was to evaluate hydration and skin parameter changes following this method of application.
Moist Skin Application
EXPERIMENTALParticipants in this group applied hyaluronic acid topically to pre-moistened skin. The goal was to assess whether applying the product to damp skin enhances its hydrating effect.
Interventions
Hyaluronic acid was applied topically to the facial skin of healthy participants once daily for a period of 3 weeks. Two application methods were used: on dry skin and on pre-moistened skin. Skin measurements were performed at baseline and after each week of intervention (Week 1, Week 2, and Week 3) to assess hydration and other skin parameters.
Eligibility Criteria
You may qualify if:
- Healthy individuals aged 18 to 50 years
- Willingness to apply the product daily for 3 weeks
- Ability to attend all scheduled skin assessments (baseline + weekly)
- Provided written informed consent
You may not qualify if:
- Known allergy or sensitivity to hyaluronic acid or any component of the product
- Active skin diseases or dermatological conditions in the facial area
- Use of systemic or topical corticosteroids or retinoids within 4 weeks prior to study
- Pregnancy or breastfeeding
- Participation in another clinical trial within the past 30 days
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Split School of Medicine
Split, Split-Dalmatia County, 21000, Croatia
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 11, 2025
First Posted
July 22, 2025
Study Start
June 18, 2025
Primary Completion
July 9, 2025
Study Completion
July 9, 2025
Last Updated
July 22, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share