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Clinical Trial Summary

This is a phase I clinical study to evaluating safety and tolerability of PRO-240 ophthalmic solution through the incidence of unexpected adverse events, as well as through changes in Best Corrected Visual Acuity (BCVA), and the incidence of stinging after its administration, compared to Optive®.


Clinical Trial Description

The variables to be evaluated include: Primary (safety): - Incidence of unexpected advere events (AE's) Secondary: - Changes in the ocular comfort index (OCI) score - Changes in intraocular pressure (IOP) - Changes in Best Corrected Visual Acuity (BCVA) - Adherence to treatment - Changes in tear film breakup time - Changes in fluorescein staining - Changes in lissamine green staining ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06375343
Study type Interventional
Source Laboratorios Sophia S.A de C.V.
Contact Alejandra Sanchez-Rios, MD
Phone 33 3001 4200
Email alejandra.sanchez@sophia.com.mx
Status Not yet recruiting
Phase Phase 1
Start date October 30, 2024
Completion date June 2025

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