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Clinical Trial Summary

The purpose of this study is to evaluate the performance of the investigational verofilcon A contact lens compared to the commercially available delefilcon A contact lens, by assessing visual acuity as the primary variable.


Clinical Trial Description

Enrolled participants will be randomized (2:1) to receive either verofilcon A (test) contact lenses or delefilcon A (control) contact lenses for wear in both eyes and attend 7 office visits: Baseline, Dispense, 1-week follow-up, 2-week follow-up, 1-month follow-up, 2-month follow-up and 3-month follow-up/Exit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03305770
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date October 12, 2017
Completion date February 21, 2018

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