A novel dietary supplement is being investigated on its potential to alleviate dry eye symptoms.

Dry Eye Syndrome (DES) affects a significant population around the world. Tear film moistens and prevents the ocular surface from dust, toxins, pollutants, etc. An imbalance in any of the tear film layers accompanied by glandular dysfunction leads to DES and it affects the ocular surface. The symptoms include discomfort, visual disturbance, inflammation, damage to ocular surface and tear film instability.

This randomized, double-blind, parallel, placebo-controlled, clinical interventional study has been designed to establish efficacy and safety of dietary supplement in adult subjects with DES. The dietary supplement formulation comprises Lutein/Zeaxanthin, Curcumin, and Vitamin D3.

There are 4 potential study visits:

• Visit 1: Screening/Baseline Visit (Day 0)
• Visit 2: First Follow-Up Visit (Day 14 ± 3 days)
• Visit 3: Second Follow-Up Visit (Day 28 ± 3 days)
• Visit 4: End of Treatment Visit (Day 56 + 3 days)

Visits will take 1 to 1.5 hours.

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