Evaluation of the Benefits of FloraGLO™ Lutein on Skin Health

Completed · Not applicable · Has a placebo group

Conditions studied: Aging, Wrinkle, Skin Elasticity, Healthy, Hydration

In brief

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.

Key facts

Study ID

NCT03769779

Run by

Kemin Foods LC

People needed

60

Starts

2019-03-06

Expected to finish

2020-03-30

Last updated by the study team

2021-02-03

Who can join

Age: 30 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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
• Using oral contraception for less than three months
• Known to be pregnant, lactating or planning to become pregnant within six months
• Unable to communicate or cooperate with the Principal Investigator due to language problems, poor mental development, or impaired cerebral function

Where it is running

• International Research Services, Inc. — Port Chester, New York, United States

Full record on ClinicalTrials.gov

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