Clinical Comparison of 4 Daily Disposable Soft Contact Lenses

Completed · Not applicable

Conditions studied: Refractive Error

In brief

The purpose of this study is to obtain on-eye performance data to inform contact lens product development and to further evaluate product performance in the intended population.

Key facts

Study ID

NCT03349632

Run by

Alcon Research

People needed

68

Starts

2018-01-10

Expected to finish

2018-02-16

Last updated by the study team

2019-02-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able to understand and must sign an approved Informed Consent Form
• Successfully wears daily disposable spherical soft contact lenses in both eyes for a minimum of 5 days per week and 8 hours per day during the past 3 months
• Best Corrected Visual Acuity of 20/25 Snellen or better in each eye
• Willing to stop wearing habitual contact lenses for the duration of study participation
• Other protocol-defined inclusion criteria may apply

You may not qualify if…

• Any eye condition, surgery, disease, or use of medication that contraindicates contact lens wear, as determined by the Investigator.
• Routinely sleeps in habitual contact lenses
• Currently wears Oasys 1-Day, MyDay, or Moist contact lenses
• Other protocol-defined exclusion criteria may apply

Where it is running

• Alcon Investigative Site — Maitland, Florida, United States
• Alcon Investigative Site — Pensacola, Florida, United States
• Alcon Investigative Site — Johns Creek, Georgia, United States

Full record on ClinicalTrials.gov

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