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Purpose

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).

Condition

Eligibility

Eligible Ages
Over 40 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Lacrifill Canalicular Filler Observational Study
  • Device: Lacrifill Canalicular Filler
    Lacrifill Canalicular Filler

Recruiting Locations

The Eye Institute of West Florida
Largo, Florida 33770
Contact:
Renee Bondurant
727-450-4668
Renee.Bondurant@eyespecialist.com

More Details

Status
Recruiting
Sponsor
The Eye Institute of West Florida

Study Contact

Renee Bondurant
727-450-4668
Renee.Bondurant@eyespecialist.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.