Evaluation of Comfort in Subjects With Moderate Dry Eye Disease

Alcon Research40 enrolled

Overview

The purpose of this study is to evaluate the comfort of an ocular lubricant in dry eye subjects. This study will be conducted in Canada and Australia.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Dry Eye

Interventions

FID123238OTHER

Lubricant applied to the ocular surface

Systane HydrationOTHER

Drops applied to the ocular surface

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Key Inclusion Criteria: * Able to understand and sign an information consent letter * Willing and able to follow instructions and maintain the appointment schedule * Has dry eye symptoms Key Exclusion Criteria: * Has suffered any ocular injury to either eye in the past 12 weeks * Is pregnant or lactating at the time of enrollment Other protocol-specified inclusion/exclusion criteria may apply.

Locations (1)

Alcon Investigator 8169

Carlton, Victoria, Australia

Outcomes

Primary Outcomes

Change from baseline in comfort rating

A visual analogue scale will be used

Time frame: Baseline, up to 12 Hours (Day 1, each product)

Data from ClinicalTrials.gov

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