Efficacy and Safety Assessment of Topical Omega Fatty Acid Product in Experimental Model of Irritant Contact Dermatitis: Randomized Controlled Trial
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Published:2024-07-23
Issue:15
Volume:14
Page:6423
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ISSN:2076-3417
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Container-title:Applied Sciences
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language:en
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Short-container-title:Applied Sciences
Author:
Ivic Magdalena1, Slugan Ana1, Leskur Dario1ORCID, Rusic Doris1ORCID, Seselja Perisin Ana1ORCID, Modun Darko1ORCID, Durdov Toni1, Bozic Josko2ORCID, Vukovic Dubravka3ORCID, Bukic Josipa1ORCID
Affiliation:
1. Department of Pharmacy, University of Split School of Medicine, 21000 Split, Croatia 2. Department of Pathophysiology, University of Split School of Medicine, 21000 Split, Croatia 3. Department of Dermatovenerology, University Hospital Split, 21000 Split, Croatia
Abstract
Contact dermatitis is a common inflammatory skin disease that often requires prescription therapy and is associated with adverse reactions. Omega fatty acids have been recognized for their anti-inflammatory effect and could serve as a safer option in contact dermatitis treatment. Therefore, the aim of this randomized controlled study, conducted at the University of Split School of Medicine, was to evaluate the efficacy and safety of omega fatty acids containing topical products in an experimental model of irritant contact dermatitis. This study was registered with ClinicalTrials (NCT06189144) and is closed. The primary outcomes were levels of transepidermal water loss, skin hydration, and skin erythema, all measured using an MPA6 device in 25 healthy participants. A significant difference was observed between the hydration values of the intervention (45.7 ± 12.4) and control groups (31.6 ± 12.3) (p < 0.05) on final measurements (day 10). Moreover, higher erythema levels were observed in participants who were smokers, compared to non-smokers. No adverse drug reactions were observed during the study period. In conclusion, omega fatty acids topical product use shows promise in the treatment of irritant contact dermatitis, and further studies are needed to evaluate efficacy in a larger sample of patients.
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