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Clinical Trial Summary

The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Biotrue ONEday contact lenses.


Clinical Trial Description

Subjects are expected to attend 3 study visits and wear the PRECISION1 and Biotrue ONEday study lenses in a crossover design for approximately 8 days of exposure to each study lens type. The expected duration of subject participation is up to 22 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04527978
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date September 15, 2020
Completion date November 6, 2020

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