Relation Between Body Mass Index and Dry Eye Disease: The Japan Public Health Center-Based Prospective Study for the Next Generation.
Ryutaro Yamanishi, Norie Sawada, Akiko Hanyuda...
https://pubmed.ncbi.nlm.nih.gov/34310488/Actively Recruiting
Led by Attikon Hospital · Updated on 2026-06-02
100
Participants Needed
1
Research Sites
8 weeks
Total Duration
This research aims to evaluate the effects of glucagon-like peptide-1 receptor agonists GLP-1 RAs on dry eye disease in patients with type 2 diabetes mellitus and obesity. Diabetes and obesity are increasing global health concerns, and these conditions are linked to eye problems like dry eye disease, which is often underdiagnosed. The study seeks to understand how newer antidiabetic medications may influence ocular surface health by assessing tear film stability and corneal changes. The study will include two groups 50 patients receiving GLP-1 receptor agonist therapy Semaglutide for overweight or obesity, with or without type 2 diabetes, and 50 control individuals matched by age, sex, and body mass index who will not receive this therapy. Participants will be observed over a period of 6 months to evaluate changes in ocular surface parameters. Participants will undergo ophthalmological assessments at two time points before starting GLP-1 RA therapy and after 6 months. These evaluations include measuring tear film break-up time, tear meniscus height, and corneal topography. Researchers will monitor changes in these ocular parameters to better understand the impact of GLP-1 RAs on dry eye disease. The study is observational and will last at least 6 months per participant.
CONDITIONS
Impact of GLP-1 Receptor Agonists on Dry Eye Disease in Patients With Type 2 Diabetes Mellitus and Obesity
V
Vaia Lambadiari, MD, PhD
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Attikon Hospital
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At baseline (single day)
Participants undergo baseline ophthalmological assessments before starting GLP-1 receptor agonist therapy or matching control observation.
1 visit (in-person)
Duration - 6 months
Participants are observed over 6 months to evaluate changes in ocular surface and tear film parameters.
1 follow-up visit (in-person) at 6 months
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Ryutaro Yamanishi, Norie Sawada, Akiko Hanyuda...
https://pubmed.ncbi.nlm.nih.gov/34310488/Attikon Hospital
Lead Sponsor