Lacrifill for Ocular Surface Optimization in Cataract Surgery

Part of paid clinical trials in Largo, Florida.

Sponsor
The Eye Institute of West Florida
Study ID
NCT07648095
Status
Recruiting
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Conditions

  • Cataract

Eligibility Criteria

Sex
ALL
Age
40 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Lacrifill Canalicular Filler — DEVICE
    Lacrifill Canalicular Filler

Study Details

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).

Key Dates

First listed
Jun 15, 2026
Start date
Jul 22, 2026
Status verified
Aug 2026
Primary completion
Jul 15, 2027
Completion
Jul 15, 2027

Study Design

Enrollment
65 participants (estimated)

Arms

  • Arm: Lacrifill Canalicular Filler
    Observational Study

Primary Outcome Measure

Mean absolute error (MAE) [ Time Frame: 1 month postoperatively ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The Eye Institute of West FloridaLargoFlorida33770
Renee Bondurant
[email protected]
727-450-4668
Neel R Desai, MD (PRINCIPAL_INVESTIGATOR)

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By research site
The Eye Institute of West Florida· Largo, FL

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