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To evaluate glaucoma patients' response to treatment with Xiidra, an FDA-approved drug for ocular surface discomfort, which will be prescribed as standard of care treatment.
To assess glaucoma patients' response to treatment with Xiidra (Lifitegrast ophthalmic solution) 5% for ocular surface discomfort caused, in part, by topical glaucoma antihypertensive medications.
Age
All ages
Sex
ALL
Healthy Volunteers
Yes
Doheny Eye Center UCLA
Fountain Valley, California, United States
Start Date
April 1, 2021
Primary Completion Date
December 1, 2026
Completion Date
December 1, 2026
Last Updated
March 13, 2026
75
ESTIMATED participants
Xiidra (Lifitegrast ophthalmic solution) 5%
DRUG
Lead Sponsor
University of California, Los Angeles
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06979752