Cellulite (Orange Peel Skin) Clinical Trial
Official title:
Safety and Efficacy of an Antioxidant Based Dietary Supplement With PUFAs in Healthy Female Volunteers With Cellulite (Orange Peel Skin)
To investigate the safety and efficacy of a dietary supplement on cellulite alleviation, fat deposits and quality of life.
The study will be conducted as a single centre, randomized, double-blind, controlled,
parallel group study with healthy female volunteers, aged 18-45 years of age, with skin
phototypes I to VI and a clinical diagnosis of cellulite on buttocks (at least score 6 at
Cellulite Severity Scale (CSS)).
The study will take 24 weeks (6 months) per subject. There will be one previsit during the
screening phase and 8 visits per subject during the treatment phase.
Safety and efficacy variables will be performed monthly.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment