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

Johnson & Johnson (J&J)

Status

Completed

Conditions

Myopia

Hyperopia

Treatments

Device: etafilcon A daily disposable soft contact lenses

Device: narafilcon B daily disposable soft contact lenses

Study type

Observational

Funder types

Industry

Identifiers

NCT01467557

CR-005059

Details and patient eligibility

About

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.

Enrollment

1,171 patients

Sex

All

Ages

8+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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.

Exclusion criteria

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.