Two Daily Disposable Contact Lenses in Symptomatic Patients

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study is to evaluate the performance of DAILIES TOTAL1® and ACUVUE OASYS® 1-DAY and with respect to visual acuity in a symptomatic study population of monthly or bi-weekly replacement lens wearers.

Key facts

Study ID

NCT03628599

Run by

Alcon Research

People needed

39

Starts

2018-08-13

Expected to finish

2018-09-25

Last updated by the study team

2019-07-05

Who can join

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

You may qualify if…

• Able to understand and must sign an IRB-approved informed consent form;
• Soft contact lens wearers in both eyes during the past 3 months;
• Best-corrected visual acuity (BCVA) 20/25 or better in each eye;
• Willing to wear study lenses at least 3 days per week and at least 8 hours per day;
• Willing to stop wearing habitual contact lenses for the duration of study participation.

You may not qualify if…

• Infection, inflammation, abnormality, condition, disease, surgery, or use of medications, as specified in the protocol;
• Intolerance, hypersensitivity, or allergy to any component of the study products;
• Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment;
• Monocular (only one eye with functional vision).

Where it is running

• Alcon Investigative Site — Bloomington, Illinois, United States
• Alcon Investigative Site — Pittsburg, Kansas, United States
• Alcon Investigative Site — Powell, Ohio, United States
• Alcon Investigative Site — Warwick, Rhode Island, United States

Full record on ClinicalTrials.gov

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