Daily Disposable Performance of 1•DAY ACUVUE® TruEye™ and 1•DAY ACUVUE® MOIST® With LACREON® TECHNOLOGY
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 8 - Any |
Updated: | 6/21/2018 |
Start Date: | October 2011 |
End Date: | October 2013 |
1•DAY ACUVUE® TruEye™ Brand Contact Lenses & 1•DAY ACUVUE® MOIST® Brand Contact Lenses With LACREON® TECHNOLOGY Daily Disposable Performance Overview Registry -TEMPO Study
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.
ACUVUE® TruEye® or 1•DAY ACUVUE® MOIST® Brand Contact Lenses with LACREON® TECHNOLOGY.
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.
We found this trial at
32
sites
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