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Clinical Trial Summary

The overall objective of this clinical study is to describe the clinical performance of the TOTAL30 soft contact lens compared to the ACUVUE OASYS with HYDRACLEAR PLUS (AOHP) soft contact lens in a daily wear modality.


Clinical Trial Description

Subjects will be expected to attend 3 visits and wear the study contact lenses at least 5 days per week and at least 8 hours per day. On Visits 2 and 3, subjects will be expected to wear the study lenses at least 6 hours prior to the study visit. The expected total duration of subject participation in the study will be approximately 1.5 months. This study will be conducted in the United Kingdom (UK). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05056987
Study type Interventional
Source Alcon Research
Contact Alcon Call Center
Phone 1-888-451-3937
Email [email protected]
Status Not yet recruiting
Phase N/A
Start date November 2021
Completion date May 2022

See also
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