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Starting soon Observational

NAION in Non-Diabetic Obese Patients Using GLP-1 Receptor Agonists: A Real-World Study

NCT07846956 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-09-21
Last updated
2026-09-29

Condition(s) studied

Non-arteritic Anterior Ischemic Optic Neuropathy ObesityObesity

Investigational drug(s) / intervention(s)

GLP-1 Receptor Agonist Therapy

GLP-1 Receptor Agonist Therapy: Use of a GLP-1 RA prescribed in routine clinical care. No study-specific treatment is given.

Study summary

Non-arteritic anterior ischemic optic neuropathy (NAION) is one of the most common causes of sudden, painless, usually unilateral vision loss in adults over 50 years of age, and no proven effective treatment exists. Glucagon-like peptide-1 receptor agonists (GLP-1 RA), such as semaglutide and tirzepatide, are widely used for type 2 diabetes and obesity. Since 2023, case series, cohort studies and regulatory reviews have raised the possibility of an association between semaglutide and NAION, but published evidence is conflicting, and data in non-diabetic obese patients are limited.

This retrospective, single-center, descriptive real-world study will review the existing records of non-diabetic obese adults (BMI \> 30) who used a GLP-1 RA and attended the ophthalmology outpatient clinic between January 2025 and February 2026 with at least two eye examinations. The aim is to describe the occurrence and time-related change of NAION and related ophthalmic findings in this population.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older * Diagnosis of obesity (body mass index \> 30) * No hearing, speech or cognitive impairment * Not receiving treatment for major depressive disorder and not using antidepressant medication * At least two eye examinations with measurements on record * Verbal agreement to participate Exclusion Criteria: • Diagnosis of diabetes * Diagnosis of hypertension * Previous optic neuritis or similar eye disease * Optic disc drusen, optic disc anomaly, glaucoma or other disease involving the optic nerve * High hyperopia or small, crowded optic disc * Not meeting the inclusion criteria or not willing to participate

Primary outcome measure(s)

  • Occurrence of NAION — Baseline (GLP-1 RA initiation) to final recorded eye examination, up to 14 months
    Number and percentage of participants with a NAION diagnosis recorded in the ophthalmic examination records.

Trial sites (1)

FacilityCityRegionStatus
Kanuni Sultan Süleyman Training and Research Hospital Istanbul Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07846956 on ClinicalTrials.gov ↗ ← All trials in Turkey