Daily Disposable Performance of 1•DAY ACUVUE® TruEye™ and 1•DAY ACUVUE® MOIST® With LACREON® TECHNOLOGY

Completed

Conditions studied: Myopia, Hyperopia

In brief

This study is an observational registry of patients who have recently been prescribed 1•DAY ACUVUE® TruEye® or 1•DAY ACUVUE® MOIST® Brand Contact Lenses with LACREON® TECHNOLOGY.

Key facts

Study ID

NCT01467557

Run by

Johnson & Johnson Vision Care, Inc.

People needed

1171

Starts

2011-10-01

Expected to finish

2013-10-01

Last updated by the study team

2018-06-19

Who can join

Age: 8 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Wearers of 1•DAY ACUVUE® TruEye™ or 1•DAY ACUVUE® MOIST® daily disposable soft contact lenses in both eyes aged >8 years of age who have recently begun use of that lens type and have purchased at least 3 month supply of lenses.
• The registrant must read and sign the Informed Consent form. Minor subjects must obtain parental signature of Informed Consent and also sign an Informed Assent Form.
• The registrant must sign the Release of Medical Records in the event of an adverse event in the study.
• The registrant must appear able and willing to adhere to the instructions set forth in this clinical protocol.

You may not qualify if…

• Previously wearing the type of lenses with which they are registering (1•DAY ACUVUE® TruEye™ or 1•DAY ACUVUE® MOIST® Daily Disposable lenses).
• Current participant in an unrelated research study.
• Employee or family member of Recruiting Practitioner or Johnson \& Johnson.

Where it is running

• Study site — Campbell, California, United States
• Study site — Fullerton, California, United States
• Study site — Huntington Beach, California, United States
• Study site — Los Angeles, California, United States
• Study site — Mountain View, California, United States
• Study site — Newport Beach, California, United States
• Study site — Salinas, California, United States
• Study site — San Francisco, California, United States
• Study site — San Francisco, California, United States
• Study site — San Francisco, California, United States
• Study site — San Jose, California, United States
• Study site — Sunnyvale, California, United States
• Study site — Washington D.C., District of Columbia, United States
• Study site — Boca Raton, Florida, United States
• Study site — Boca Raton, Florida, United States
• Study site — Fort Lauderdale, Florida, United States
• Study site — Fort Lauderdale, Florida, United States
• Study site — North Miami, Florida, United States
• Study site — Pembroke Pines, Florida, United States
• Study site — Wellington, Florida, United States
• Study site — Roswell, Georgia, United States
• Study site — Des Moines, Iowa, United States
• Study site — Shreveport, Louisiana, United States
• Study site — Belmont, Massachusetts, United States
• Study site — Cambridge, Massachusetts, United States

Full record on ClinicalTrials.gov

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