Evaluation of Comfort in Symptomatic Contact Lens Wearers

Alcon

Status: Completed

Conditions: Ocular Comfort

Treatments: Other: FID123238

Study type: Interventional

Funder types: Industry

Identifiers

NCT04963543

DEJ475-E003

Details and patient eligibility

About

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.

Full description

The duration of individual participation is six days.

Enrollment: 17 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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17 participants in 1 patient group

FID123238

Experimental group

Description:

FID123238 applied to the ocular surface, 1 application per day, for five consecutive days

Treatment:

Other: FID123238