Clinical Trial

A Study to Evaluate Corneal Endothelial Cell Density (ECD) in Subjects With Dry Eye Disease (DED) Administering Miebo® (Perfluorohexyloctane Ophthalmic Solution) for 12 Months.

Active, Not Recruiting Phase 4
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Record status
This record was last updated December 17, 2024 (before its estimated November 2025 completion). Its status may not reflect the trial's current state.
Summary
A Randomized, Multicenter, Double-Masked, Saline-Controlled Trial to Evaluate Corneal Endothelial Cell Density in Subjects With Dry Eye Disease Administering Miebo® (Perfluorohexyloctane Ophthalmic Solution) for 12 Months
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-08-21.
Status change: Recruiting → Active, Not Recruiting 2024-12-16
Trial Details
NCT Number NCT06565650
Lead Sponsor Bausch & Lomb Incorporated
Conditions Dry Eye
Enrollment 216 participants
Start Date 2024-07-31
Primary Completion 2025-11 (estimated)
Study Completion 2025-11 (estimated)
Updated on ClinicalTrials.gov 2024-12-17