Clinical Performance Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens

Completed · Not applicable

Conditions studied: Refractive Errors

In brief

The purpose of this study is to obtain on-eye performance data to inform contact lens product development.

Key facts

Study ID

NCT04055519

Run by

Alcon Research

People needed

36

Starts

2019-09-19

Expected to finish

2019-12-03

Last updated by the study team

2021-05-13

Who can join

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

You may qualify if…

• Sign Informed Consent document.
• Successful wear of spherical weekly/monthly soft contact lenses in both eyes for a minimum of 5 days per week and 8 hours per day during the past 3 months.
• Possess spectacles that provide a corrected visual acuity of 20/40 or better in both eyes.
• Other protocol-specified inclusion criteria may apply.

You may not qualify if…

• Any eye condition or disease or use of medication that contraindicates contact lens wear.
• Eye surgery, irregular cornea, eye injury as specified in the protocol.
• Routinely sleeps in contact lenses at least 1 night per week over the last 3 months prior to enrollment.
• Any use of topical ocular medications, artificial tear or rewetting drops that would require instillation during contact lens wear.
• Habitually wears Biofinity contact lenses.
• Other protocol-specified exclusion criteria may apply.

Where it is running

• Alcon Investigative Site — Maitland, Florida, United States
• Alcon Investigative Site — Bloomington, Illinois, United States
• Alcon Investigative Site — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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