Dry Eye Clinical Trial - CEQUA for Sjogren's Syndrome Dry Eye

Status Completed

Clinical Trial Summary

The primary objective of this study is to show that CEQUA (cyclosporine 0.09% ophthalmic solution) improves symptoms of dry eye disease in a population of patients with Sjogren's Syndrome diagnosis.

Clinical Trial Description

After being informed about the study and potential risks, all participants giving informed consent will have an eye exam and will be asked about their medical history to determine eligibility for the study. Eligible participants will continue to the second visit the same day or up to 10 days later. During the second visit participants will answer questionnaires about their eyes and have their vision, eyes, and tears examined. All participants will be given CEQUA to use over the duration of the study. The same procedures will be repeated every four weeks for 3 months total. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04835623
Study type	Interventional
Source	Center for Ophthalmic and Vision Research, LLC
Contact
Status	Completed
Phase	Phase 4
Start date	June 21, 2021
Completion date	March 21, 2024

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