Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensive Medication Use

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The objective of this study is to evaluate whether reduction in topical medication with the injection of a sustained release capsule (Durysta) leads to a reduction in ocular surface inflammation, indicated by levels of caspase-1, an inflammatory biomarker.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Eye with open-angle glaucoma or suspected of open-angle glaucoma

• Pseudophakic in eye of interest with Shafer grading ≥3

• ≤ 3 daily applications of topical glaucoma medications for ≥6 months (of which one is a nightly preserved PGA)

• Good adherence to medication regimen - screening questions to be asked of potential subject:

• In the last month, what percentage of the time would you estimate missing the application of drops? (Must be ≤20%)

• When was the last administration? (Last dose must have been within last 24 hours)

• Presence of punctate epithelial erosions in the cornea (NEI scale \> 3)

Locations
United States
Florida
Bascom Palmer Eye Institute
RECRUITING
Miami
Contact Information
Primary
Javier Paredes, BA, MBA
jxp2537@med.miami.edu
305-326-6387
Backup
Monica Arango, BA
mrarango@med.miami.edu
305-326-6351
Time Frame
Start Date: 2026-03
Estimated Completion Date: 2028-01-31
Participants
Target number of participants: 20
Treatments
Experimental: Durysta
Participants will receive a one-time intracameral administration of Durysta - bimatoprost 10mcg
Sponsors
Collaborators: AbbVie
Leads: University of Miami

This content was sourced from clinicaltrials.gov

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