A Clinical Evaluation of an Investigational Lubricant Eye Gel (FID 115958D)

Alcon Research147 enrolled

Overview

The purpose of this study is to estimate the change in sodium fluorescein staining, as a sign of dry eye, during six weeks of treatment with FID 115958D or Refresh Liquigel.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

147

Conditions

Dry Eye

Interventions

Lubricant Eye DropOTHER

1 drop in each eye, four times a day for 42 days

Refresh LiquigelOTHER

1 drop in each eye, four times a day for 42 days

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Documented diagnosis of dry eye * NaFl Corneal staining sum score ≥ 3 in either eye * Current use of a lubricant eye gel or ointment at least once per week (over the previous month) Exclusion Criteria: * No contact lenses wear throughout the study period * Must not have had punctal plugs inserted within 30 days preceding enrollment

Outcomes

Primary Outcomes

Corneal Staining

Time frame: Day 42

Data from ClinicalTrials.gov

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