Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers

Alcon Research36 enrolled

Overview

The purpose of this study is to evaluate the ocular comfort of 3 ocular lubricants and a comparator.

The expected duration of subject participation is at least 7 days. This study will be conducted in Australia and Canada.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Dry Eye

Interventions

OTF Ocular LubricantOTHER

Ocular lubricant in 1 of 3 test formulations

Ocular LubricantOTHER

Commercially available ocular lubricant

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Key Inclusion Criteria: * Is able to understand and sign an approved information consent letter; * Habitually wears daily disposable soft contact lenses in both eyes * Uses rewetting drops on a regular basis; * Other protocol-defined inclusion criteria may apply. Key Exclusion Criteria: * Routinely sleeps in habitual contact lenses; * Has any known active ocular disease and/or infection; * Is pregnant or lactating; * Other protocol specified exclusion criteria may apply.

Locations (3)

School of Optometry and Vision

Sydney, New South Wales, Australia

Deakin Collaborative Eye Care Clinic, Deakin University

Waurn Ponds, Victoria, Australia

School of Optometry and Vision Science, University of Waterloo

Waterloo, Ontario, Canada

Outcomes

Primary Outcomes

Ocular comfort

Comfort will be rated using a visual analog scale (0-100) from 0-100, where 0=poor and 100=excellent.

Time frame: Up to Day 5

Data from ClinicalTrials.gov

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