Evaluation of Lacrifill™ Canalicular Filler for Optimization of Ocular Surface Parameters and Biometric Precision in Prospective Cataract Surgery Patients With Dry Eye Disease
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:
• 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
Locations
United States
Florida
The Eye Institute of West Florida
RECRUITING
Largo
Contact Information
Primary
Renee Bondurant
Renee.Bondurant@eyespecialist.com
727-450-4668
Time Frame
Start Date: 2026-07-22
Estimated Completion Date: 2027-07-15
Participants
Target number of participants: 65
Treatments
Lacrifill Canalicular Filler
Observational Study
Related Therapeutic Areas
Sponsors
Leads: The Eye Institute of West Florida
Collaborators: Sengi