Evaluation of Comfort in Symptomatic Contact Lens Wearers

Alcon Research17 enrolled

Overview

The purpose of this study is to evaluate the comfort of an ocular lubricant in symptomatic contact lens wearers. This study will be conducted in Canada.

The duration of individual participation is six days.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Ocular Comfort

Interventions

FID123238OTHER

Lubricant applied to the ocular surface

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; * Is able to achieve 20/40 or better monocular VA with habitual contact lenses; * Has a pair of spectacles for vision correction. * 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-defined exclusion criteria may apply.

Locations (1)

Alcon Investigative Site 6189

Waterloo, Ontario, Canada

Outcomes

Primary Outcomes

Comfort, collected for each eye

A visual analogue scale will be used

Time frame: Up to Day 6

Data from ClinicalTrials.gov

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