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Clinical Trial Summary

The purpose of this study is to compare ease of handling and vision acuity of two multifocal contact lenses to correct presbyopia that are currently CE marked and on the UK market.


Clinical Trial Description

This is an interventional, prospective, open label, sequential design study. Participants will wear each study contact lens on a daily disposable wearing modality for 14 ± 3 days and attend the clinic for a total of three study visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06328660
Study type Interventional
Source Coopervision, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date February 15, 2024
Completion date June 18, 2024

See also
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