Evaluation of Wear Experience With a Daily Disposable Contact Lens

Ohio State University30 enrolled

Overview

To evaluate the wear experience of current two-week contact lens wearers after they have been fit into a daily disposable contact lens. This is a single arm, non-comparative study.

This is a single arm, non-comparative study. All participants were habitual lens wearers of the same brand of lenses, and were re-fit with the study lenses.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Contact Lens

Interventions

Daily Disposable Contact LensDEVICE

Soft, daily disposable spherical contact lens used to correct distance vision.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Must be current Acuvue® Oasys® spherical contact lens wearers. * Distance visual acuity of 20/25 or better with current contact lenses. * Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI). * Ability to give informed consent. * Willing to spend time for the study, which includes attending two study visits and wearing contact lenses on days between study visits. * Either gender. * Any racial or ethnic origin. Exclusion Criteria: * No current ocular inflammation or infection. * Not currently pregnant or lactating.

Locations (1)

The Ohio State University College of Optometry

Columbus, Ohio, United States

Outcomes

Primary Outcomes

Contact Lens Dry Eye Questionnaire (CLDEQ-8) Survey

Participants complete the Contact Lens Dry Eye Questionnaire (CLDEQ-8) survey. This is an 8 question survey assesses symptoms while wearing contact lenses with possible scores from 0 (no symptoms) to 37 (maximum symptoms). Higher scores indicate worsening symptoms of dry eye while wearing lenses.

Time frame: 2 weeks

Data from ClinicalTrials.gov

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