Lacrifill for Ocular Surface Optimization in Cataract Surgery

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Conditions studied: Cataract

In brief

This is a single-site observational study designed to evaluate the efficacy of Lacrifill™ canalicular filler in optimizing ocular surface parameters and biometric precision in prospective cataract surgery patients with dry eye disease (DED).

Key facts

Study ID

NCT07648095

Run by

The Eye Institute of West Florida

People needed

65

Starts

2026-07-15

Expected to finish

2027-07-15

Last updated by the study team

2026-06-15

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age >= 40 years
• Diagnosed dry eye (OSDI >= 13, TBUT < 10 sec, or Oxford staining >= Grade 2)
• No recent ocular surgeries (<6 months)
• No significant changes in DED regimen within last 1 month

You may not qualify if…

• Previous punctal plugs or canalicular cautery
• Active ocular inflammation or corneal pathology unrelated to DED

Where it is running

• The Eye Institute of West Florida — Largo, Florida, United States

Full record on ClinicalTrials.gov

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