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Clinical Trial Summary

The primary objective of this study is to evaluate the overall performance of an investigational silicone hydrogel lens when compared to ACUVUE OASYS® with HYDRACLEAR® PLUS (AOHP).


Clinical Trial Description

Part A of this study is a randomized, double masked, crossover study comparing 2 contact lens products. The expected duration of subject participation in Part A is approximately 8 weeks with 5 scheduled visits. Part B of this study is a non-randomized, single masked, single group study with 1 contact lens product. The expected duration of subject participation in Part B is approximately 4 weeks with 3 scheduled visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04532099
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date September 9, 2020
Completion date May 4, 2021

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