NCT02388763

Clinical Evaluation of MyDay™ and 1-DAY ACUVUE® TruEye®

Clinical Evaluation of MyDay™ Daily Disposable Silicone Hydrogel Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 66 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to evaluate the functional vision of 2 daily disposable silicone hydrogel contact lenses using Time Controlled Visual Acuity (TCVA) measurements at high luminance and high contrast after 10+/-3 days of wear post 3 hour exposure to a reduced humidity environment.

Detailed description

After randomization, participants attended a baseline visit to include a 3 hour exposure to reduced humidity environment. The participant's habitual lenses were worn for the baseline visit.

Conditions

• Refractive Error

Interventions

Type	Name	Description
DEVICE	Stenfilcon A contact lenses	Contact lenses worn during Period 1 or 2, as randomized
DEVICE	Narafilcon A contact lenses	Contact lenses worn during Period 1 or 2, as randomized

Timeline

• Start date: 2015-04-01
• Primary completion: 2015-09-01
• Completion: 2015-09-01
• First posted: 2015-03-17
• Last updated: 2016-12-05
• Results posted: 2016-10-19