CyanthOx™ Capsule Efficacy Study

Clinical Study Plan for CyanthOx™ Hard Capsule

The goal of this clinical trial is to learn whether daily intake of CyanthOx™80 capsules can improve skin, scalp, hair, and selected blood biomarkers in healthy adults after 12 weeks.

Researchers will compare participants who take CyanthOx™80 with participants who take a placebo to evaluate its effectiveness and tolerability.

A total of 40 participants will be randomly assigned to the CyanthOx™80 group or placebo group, with 20 participants in each group. Participants will not know which capsule they receive.

Participants will:

Take one capsule daily for 12 weeks. Attend study visits at baseline and weeks 4, 8, and 12. Undergo non-invasive facial skin assessments at baseline, week 4, and week 12. Undergo scalp and hair assessments at baseline and weeks 4, 8, and 12. Provide a 10 mL blood sample at baseline and week 12 for tests related to antioxidant capacity, inflammation, aging, collagen, and blood lipids.

Complete questionnaires about skin condition and product satisfaction. Provide collected shed hair at weeks 4, 8, and 12. Have facial, scalp, and hair photographs taken. Identifiable areas will be masked before disclosure.

Before each skin or scalp assessment, participants will cleanse the test area with water and rest at room temperature for 30 minutes.

Inclusion Criteria:

• Participants aged over 18 years.

Exclusion Criteria:

• Individuals who are unwilling to participate voluntarily.
• Individuals diagnosed by a physician with skin disease, liver cirrhosis, or chronic renal failure.
• Individuals with known allergies to cosmetics, drugs, or foods.
• Pregnant or breastfeeding individuals.
• Individuals taking medications for chronic diseases.
• Students taught by the principal investigator.
• Individuals unwilling to allow their study-related photographs to be disclosed. Vegetarians.