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Safety and Efficacy of a Dietary Supplement in Females With Cellulite

NCT01321268 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2015-06-08

No results posted yet for this study

Summary

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

Conditions

  • Cellulite (Orange Peel Skin)

Interventions

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

Sponsors & Collaborators

  • DSM Nutritional Products, Inc.

    lead INDUSTRY

Principal Investigators

  • Doris M Hexsel, MD · Brazilian Center for Studies in Dermatology (CBED)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2012-07-31
Completion
2012-07-31

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01321268 on ClinicalTrials.gov