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Clinical Trials/NCT03769779
NCT03769779
Completed
Not Applicable

A 12-Week, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Benefits of FloraGLO™ Lutein on Skin Health

Kemin Foods LC1 site in 1 country60 target enrollmentMarch 6, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
Kemin Foods LC
Enrollment
60
Locations
1
Primary Endpoint
Objective Skin Hydration
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Therefore, the present study is designed to contribute to the body of literature by investigating the effect of 12-weeks of lutein supplementation on multiple parameters of skin health and appearance in healthy women.

Detailed Description

This is a randomized, double-blind, placebo-controlled, parallel twelve-week study of the performance of an oral test product to evaluate the effects of twelve weeks of lutein supplementation on skin health and appearance in healthy women. A seven-day washout period will precede the evaluation period. The subjects in each cohort will use consume one softgel of their assigned test product (treatment or placebo) daily in the morning with breakfast for 12 weeks. Changes in skin condition and appearance as well as blood chemistry will be assessed using results from expert visual grading, instrumental assessments, skin and blood assays and subjective questionnaire responses. Subjects will be recruited during the winter season to account for seasonal variations of skin parameters. Evaluation points will occur pre-application (Baseline; Week 0) and after 42 and 84 days of use (D42, D84; Week 6, Week 12). Data will be collected on the following outcomes: 1. Skin Hydration 2. Skin texture/smoothness 2. Reduction of facial fine lines and wrinkles 3. Skin elasticity and firmness 4. Sagging skin, dry skin, skin tone, appearance from expert clinical grading and subjective questionnaire responses. 6. Skin hydration 7. Skin collagen 8. Skin lipid content. 9. Skin Carotenoids

Registry
clinicaltrials.gov
Start Date
March 6, 2019
End Date
March 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Kemin Foods LC
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Females in good health, and between the ages of 30 and 65 years old
  • Fitzpatrick Skin Type I-V
  • Mild to moderate loss of skin elasticity, wrinkles (global) and rough skin texture
  • Able to read, understand and sign an informed consent form
  • Willing and able to follow all study directions, attend study visits as scheduled and willing to accept the restrictions of the study
  • Willing and able to maintain regular diet, exercise, hydration, and sleep patterns throughout the study

Exclusion Criteria

  • Participating in any other clinical study
  • Acute or chronic disease or medical condition
  • Unreliable or unlikely to be available for the duration of the study
  • Routine use of tanning bed(s)
  • History of abnormal response to sunshine
  • Current usage of medications with contraindication of enhancing sun exposure, or medications for skin conditions.
  • History of allergic reactions, skin sensitization and/or known allergies to cosmetic ingredients, toiletries, sunscreens, etc.
  • Immunocompromised subjects
  • Subject has a history of unconventional sleep patterns
  • Started Hormone Replacement Therapy within the last three months

Outcomes

Primary Outcomes

Objective Skin Hydration

Time Frame: ANOVA including weeks 6 and 12

Corneometer Value

Subjective Skin Hydration

Time Frame: ANOVA including weeks 6 and 12

Subjective Questionnaire Visual Analog Scale

Secondary Outcomes

  • Objective Skin Texture(ANOVA including weeks 6 and 12)
  • Objective Facial Lines and Wrinkles(ANOVA including weeks 6 and 12)
  • Skin Collagen SIAsScope(ANOVA including weeks 6 and 12)
  • Skin Carotenoids(ANOVA including weeks 6 and 12)
  • Subjective Facial Lines and Wrinkles(ANOVA including weeks 6 and 12)
  • Skin Collagen Ultrasound(ANOVA including weeks 6 and 12)
  • Subjective Skin Texture(ANOVA including weeks 6 and 12)
  • Objective Skin elasticity(ANOVA including weeks 6 and 12)
  • Skin Lipids(ANOVA including weeks 6 and 12)
  • Objective Sagging skin, dry skin, skin tone, and overall appearance(ANOVA including weeks 6 and 12)
  • Subjective Skin elasticity(ANOVA including weeks 6 and 12)
  • Subjective Sagging skin, dry skin, skin tone, and overall appearance(ANOVA including weeks 6 and 12)

Study Sites (1)

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