NCT01321268

Safety and Efficacy of a Dietary Supplement in Females With Cellulite

Safety and Efficacy of an Antioxidant Based Dietary Supplement With PUFAs in Healthy Female Volunteers With Cellulite (Orange Peel Skin)

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 8 (actual)
• Sponsor: dsm-firmenich Switzerland AG · Industry
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: Accepted

Summary

To investigate the safety and efficacy of a dietary supplement on cellulite alleviation, fat deposits and quality of life.

Detailed description

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.

Conditions

• Cellulite (Orange Peel Skin)

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	dietary supplement for cellulite (PUFA, resveratrol, lycopene, beta carotene, lutein)	oral, twice daily in morning and evening for 6 months
DIETARY_SUPPLEMENT	Viatmin E	oral, twice daily in morning and evening for 6 months

Timeline

• Start date: 2011-05-01
• Primary completion: 2012-07-01
• Completion: 2012-07-01
• First posted: 2011-03-23
• Last updated: 2015-06-08

Locations

1 site across 1 country: Brazil