Clinical evaluation of DAILIES TOTAL 1 performance in a Japanese population.
Not Applicable
- Conditions
- Habitual current daily disposable soft contact lenses wearers with symptoms of contact lens discomfort.
- Registration Number
- JPRN-UMIN000021976
- Lead Sponsor
- Alcon Japan Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Currently wearing DAILIES TOTAL 1 or 1-DAY ACUVUE TruEye sphere lenses. Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear. Use of systemic or ocular medications in which contact lens wear could be contraindicated as determined by the investigator. Eye injury or surgery within 12 weeks immediately prior to enrollment. History of herpetic keratitis, ocular surgery or irregular cornea. Prior refractive surgery. Monocular (only 1 eye with functional vision) or fit with only 1 lens. Participation in any clinical trial within 30 days of the enrollment visit. Other protocol-specified exclusion criteria may apply.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Investigator-rated successful lens centration of Optimal after 7 to 13 days of wearing.
- Secondary Outcome Measures
Name Time Method