Effect of a Dietary Supplement on Gut Microbiota and Ocular Surface Outcomes in Dry Eye Disease

NARecruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

September 1, 2025

Primary Completion Date

November 15, 2025

Study Completion Date

January 30, 2026

Conditions
Dry EyeAge-Related Macular Degeneration (AMD)Age-related Macular Degeneration (ARMD)
Interventions
DIETARY_SUPPLEMENT

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.

Trial Locations (1)

Unknown

RECRUITING

Medipol University, Istanbul

All Listed Sponsors
collaborator

Istanbul Medipol University Hospital

OTHER

collaborator

Liv Hospital (Ulus)

UNKNOWN

lead

Varol TUNALI

INDUSTRY

NCT07148271 - Effect of a Dietary Supplement on Gut Microbiota and Ocular Surface Outcomes in Dry Eye Disease | Biotech Hunter | Biotech Hunter