Design Validation of Senofilcon A With New UV-blocking Additive

Clinical Trial Summary

This is a 2-visit, multi-site, partially subject-masked, 2-arm parallel, controlled, randomized and dispensing trial. Subjects will be randomized to one of two study lenses for the entire duration of the study. The study lenses will be worn for a period of 2 weeks each in a bilateral fashion.

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NCT number	NCT03707821
Study type	Interventional
Source	Johnson & Johnson Vision Care, Inc.
Contact
Status	Completed
Phase	N/A
Start date	October 1, 2018
Completion date	November 1, 2018

Design Validation of Senofilcon A With New UV-blocking Additive

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms