A Dispensing Clinical Trial of Comfilcon A Extended Range Multifocal Lenses

Completed · Not applicable

Conditions studied: Presbyopia

In brief

The aim of this study is to validate the clinical of comfilcon A extended range high add center near (CN) multifocal lenses in existing contact lens wearers against the current comfilcon A high add multifocal lenses.

Key facts

Study ID

NCT02719353

Run by

CooperVision, Inc.

People needed

14

Starts

2016-03-01

Expected to finish

2016-08-01

Last updated by the study team

2020-07-30

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• A person is eligible for inclusion in the study if he/she:
• Has had a self-reported oculo-visual examination in the last two years
• Is 50 years of age or greater and has full legal capacity to volunteer
• Is able to read and understand the informed consent
• Is willing and able to follow instructions and maintain the appointment schedule
• Has a spherical distance contact lens prescription between -1.00 and -5.00D (Diopters) (inclusive)
• Near Add Power requirement of +2.25D or greater
• Has spectacle cylinder 0.75 D in both eyes
• Has normal binocularity (no amblyopia, no strabismus, no habitually uncorrected anisometropia ≥ 2.00D)
• Has monocular best-corrected distance visual acuity of 20/30 or better in each eye
• Has clear corneas and no active ocular disease
• Has not worn gas permeable contact lenses for 1 month prior to the study

You may not qualify if…

• A person will be excluded from the study if he/she:
• Has never worn contact lenses before
• Has any systemic disease affecting ocular health
• Is using any systemic or topical medications that will affect ocular health
• Has any ocular pathology or abnormality that would affect the wearing of contact lenses
• Is aphakic (i.e. missing their natural lens inside their eye)
• Has uncorrected anisometropia (i.e. difference in the prescription between the eyes) of ≥2.00 D
• Has undergone corneal refractive surgery
• Is participating in any other type of eye related clinical or research study.

Where it is running

• CORL, Indiana University — Bloomington, Indiana, United States

Full record on ClinicalTrials.gov

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