Study detail
Recruiting
Evaluation of Lacrifill™ Canalicular Filler for Optimization of Ocular Surface Parameters and Biometric Precision in Prospective Cataract Surgery Patients With Dry Eye Disease
The Eye Institute of West Florida
Summary
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).
Eligibility
- Age range
- 40+ years
- Sex
- All
- Healthy volunteers
- No
Detailed criteria
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
Interventions
- DeviceLacrifill Canalicular Filler
Lacrifill Canalicular Filler
Location
- The Eye Institute of West FloridaLargo, Florida