A Study to Assess the Impact of a Nutritional Supplement on Wellbeing and Nutrient Absorption

Enrolling by invitation · Not applicable · Has a placebo group

Conditions studied: Nutrition Status

In brief

The objective of this placebo controlled randomized research is to demonstrate the health benefits of a carotenoid nutritional supplement as compared to placebo in terms of nutrient levels, quality of life, feelings, of wellness, brain health, energy, immunity, and appearance.

Key facts

Study ID

NCT06749808

Run by

Pharmanex

People needed

36

Starts

2024-12-01

Expected to finish

2025-02-01

Last updated by the study team

2024-12-31

Who can join

Age: 20 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects male or female age 20-65 years old.
• Subjects who score 30,000 or below on the Pharmanex BioPhotonic Scanner.
• Subjects of Fitzpatrick skin types I-VI with no known medical conditions that, in the investigator's opinion, may interfere with study participation.
• Subjects must be able to read, understand and provide written informed consent.
• Individuals must agree to continue to use all regular brands of cosmetics and the assigned test materials for the duration of the study. Individuals must refrain from using any new products other than the assigned test supplements.
• Subjects must agree to avoid excessive sun exposure (no more than 10-15 minutes of direct sunlight without SPF protection) and the use of artificial tanning methods for the duration of the study.

You may not qualify if…

• 1. Individuals who are participating in any other research study. 2. Subjects who are regularly taking oral nutritional supplements containing carotenoids as specified by the sponsor.
• Subjects who have demonstrated a previous hypersensitivity reaction to any of the ingredients of the study supplement.
• Concurrent therapy with any medication either topical or oral that might interfere with the study.
• Subjects who are alcohol or narcotic addicts. 6. Subjects who are unwilling to leave their current oral medications unchanged for the duration of the study.
• Subjects who use an indoor tanning booth. 8. Subjects, who are pregnant, breast feeding or planning a pregnancy. 9. Subjects with clinically significant unstable medical disorders, such as cancer, diabetes, neurodegenerative disorders, active autoimmune disease, liver or kidney disease, schizophrenia, depression, other major mental illness.
• Subjects who are cigarette smokers. 11. Subjects who regularly use supplements containing >2mg carotenoids such as: LifePak, Beauty Focus Collagen+, ageLOC Youth.
• Subjects who are unwilling or unable to comply with the requirements of the protocol.
• Subjects who are participating in another similar research study.

Where it is running

• Nu Skin — Provo, Utah, United States

Full record on ClinicalTrials.gov

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