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Study to Evaluate the Effect of a Nu Skin Product and Device for Brown Spots

NCT01149876 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2014-11-06

Study results available
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Summary

The purpose of this study is to determine whether a topical Nu Skin product with or without a galvanic spa device improves brown spots on the face. The Nu Skin product will be compared to an over the counter moisturizer and tretinoin cream.

Conditions

  • Hyperpigmentation

Interventions

OTHER

Nu Skin Product

Thin layer of Nu Skin product applied to face.

OTHER

Cosmetic instrument

Cosmetic instrument with topical Nu Skin product. Thin layer of Nu Skin product applied to face followed by galvanic, used for 3 minutes.

DRUG

Tretinoin cream 0.05

Thin layer of tretinoin applied to face.

OTHER

CeraVe moisturizer

Thin layer of CeraVe applied to face.

Sponsors & Collaborators

  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Molly Wanner, MD · MGH

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • United States

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 NCT01149876 on ClinicalTrials.gov