Clinical Performance of Three Daily Disposable Silicone Hydrogel Contact Lenses
- Conditions
- Visual Acuity
- Registration Number
- NCT06778057
- Lead Sponsor
- Johnson & Johnson Vision Care, Inc.
- Brief Summary
This is a subject-masked, randomized, prospective, bilateral, 3x3 crossover dispensing clinical investigation to assess the clinical performance of a new lens type comparison.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 23
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Lens Fit Acceptance Follow-up assessments will be made approximately 8-10 hours after lens dispensing Lens Fit Acceptance: Lens fit acceptance will be assessed at dispensing and follow-up visits for each subject eye.
An unacceptable fit is deemed by one or more of the following criteria:
* limbal exposure at primary gaze or with extreme eye movement.
* edge lift.
* excessive movement with blink in primary gaze.
* insufficient movement with blink in upgaze.
* insufficient movement in push-up test.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
The University of Manchester, Department of Optometry & Neuroscience
🇬🇧Manchester, United Kingdom
The University of Manchester, Department of Optometry & Neuroscience🇬🇧Manchester, United Kingdom