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Lacrifill for Ocular Surface Optimization in Cataract Surgery

Evaluation of Lacrifill™ Canalicular Filler for Optimization of Ocular Surface Parameters and Biometric Precision in Prospective Cataract Surgery Patients With Dry Eye Disease

Who can join

Ages 40 and older · All sexes

Inclusion Criteria:

* 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

Exclusion Criteria:

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

About the study

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).

What is being tested

• Lacrifill Canalicular Filler (device)

Sponsor: The Eye Institute of West Florida · Participants: 65 · Started: Jul 22, 2026

Contact the study team

• Renee Bondurant · Phone: 727-450-4668

Official record on ClinicalTrials.gov — NCT07648095

Locations in the U.S.

Conditions

• Cataract

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.