Lacrifill for Ocular Surface Optimization in Cataract Surgery
ConditionCataract
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40+
SponsorThe Eye Institute of West Florida
About this trial
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 criteria
Qualifiers
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
Disqualifiers
Previous punctal plugs or canalicular cautery
Active ocular inflammation or corneal pathology unrelated to DED
Trial design
Treatments tested in this trial
- Lacrifill Canalicular Filler
Treatment groups
65 Participants
are divided into 1 treatment groupSponsors and collaborators
The Eye Institute of West Florida
Lead sponsor
Sengi
Collaborator
Source ClinicalTrials.gov