Clinical Evaluation of Two Daily Disposable Lenses in Neophytes

CIBA VISION326 enrolled

Overview

The purpose of this study is to evaluate the performance of two daily disposable contact lenses in a population of neophytes (new wearers).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

326

Conditions

Myopia

Interventions

nelfilcon A contact lensDEVICE

Commercially marketed, hydrogel, single-vision contact lens for daily wear, daily disposable use.

narafilcon A contact lensDEVICE

Commercially marketed, silicone hydrogel, single-vision contact lens for daily wear, daily disposable use.

Eligibility

Sex: ALLMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: * No previous contact lens experience or attempts to try contact lenses (neophytes). * Currently wearing spectacles or needing vision correction in both eyes. * No older than 45 years of age. * Able to achieve visual acuity of at least 20/40 in each eye with study lenses in the available parameters. * Interested in wearing contact lenses. * Willing to wear study lenses for at least 8 hours/day, at least 5 days/week. * Other protocol-defined inclusion/exclusion criteria may apply. Exclusion Criteria: * Eye injury or surgery within twelve weeks prior to enrollment. * Pre-existing ocular irritation that would preclude contact lens fitting. * Previous corneal or refractive surgery. * Currently enrolled in any Clinical Trial. * Other protocol-defined inclusion/exclusion criteria may apply.

Locations (1)

The Research Intelligence Group (TRiG)

Fort Washington, Pennsylvania, United States

Outcomes

Primary Outcomes

Overall Lens Satisfaction

Overall Lens Satisfaction, as interpreted by the participant and reported on a questionnaire as a single, retrospective evaluation of 1-week's wear time. Overall lens satisfaction was measured on a 10-point scale, with 1 being Poor and 10 being Excellent

Time frame: 1 week

Data from ClinicalTrials.gov

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