Nanodropper Use in Primary Open-Angle Glaucoma Patients: A Non-Inferiority Trial
This randomized, single-masked, crossover, non-inferiority trial aims to evaluate the safety and efficacy of Nanodropper-mediated microdrops of ocular hypotensive topical treatments (experimental intervention) compared to standard drops of the same medication(s) (active comparator) in Wilford Hall Ambulatory Surgical Center (WHASC) primary open-angle glaucoma (POAG) and ocular hypertension (OHTN) patients.
Conditions studied
Ocular Hypertension, Primary Open Angle Glaucoma
About this study
This randomized, single-masked, crossover, non-inferiority trial aims to evaluate the safety and efficacy of Nanodropper-mediated microdrops of ocular hypotensive topical treatments (experimental intervention) compared to standard drops of the same medication(s) (active comparator) in Wilford Hall Ambulatory Surgical Center (WHASC) primary open-angle glaucoma (POAG) and ocular hypertension (OHTN) patients.
Interventions
- Device: Nanodropper — Nanodropper delivers 1/5 of eye drop volume compared to regular droppers
- Device: Regular dropper — Delivers full eye drop volume
Primary outcomes
- Change from baseline in mean intraocular pressure at 6 month (Change from baseline to month 6)
Eligibility information
Study locations
- Wilford Hall Ambulatory Surgical Center, Lackland Air Force Base, Texas 78236 United States
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-11-03.