30
Participants
Start Date
September 1, 2025
Primary Completion Date
November 15, 2025
Study Completion Date
January 30, 2026
Dietary Supplement Product
Participants will receive a dietary supplement product administered orally once daily for 8 weeks. The supplement is provided in capsule form and taken with water. The intervention is designed to modulate gut microbiota composition and diversity, with the potential to influence ocular surface outcomes in patients with dry eye disease. The regimen will be self-administered at home, with adherence monitored at study visits. Stool samples will be collected at baseline and week 8 for metagenomic sequencing, and ocular surface parameters will be assessed at the same time points. Safety will be evaluated by monitoring for adverse events throughout the intervention period.
RECRUITING
Medipol University, Istanbul
Istanbul Medipol University Hospital
OTHER
Liv Hospital (Ulus)
UNKNOWN
Varol TUNALI
INDUSTRY