NCT02500368

A Dispensing Clinical Trial of a Study Test Silicone Hydrogel Lens Against Control Lens Over 1 Week

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 41 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 17 Years
• Healthy volunteers: Not accepted

Summary

This is a 1-week dispensing, double-masked, randomized, bilateral study comparing the test lens against the control lens.

Detailed description

The order of lens wear (test lens first, control lens second or control lens first, test lens second) will be selected according to a randomization table. Both test and control lenses will be used in a daily wear modality for 1 week. It is anticipated that this study will involve following visits: Baseline (screening and dispense of 1st study pair of lenses, visit combined), 1-week visit (follow-up of the 1st study pair of lenses and dispense the 2nd study pair of lenses) and 2-week visit (1 week follow-up of the 2nd study pair of lenses).

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	silicone hydrogel lens (test)	contact lens
DEVICE	enfilcon A lens (control)	contact lens

Timeline

• Start date: 2015-07-01
• Primary completion: 2015-08-01
• Completion: 2015-09-01
• First posted: 2015-07-16
• Last updated: 2020-07-29
• Results posted: 2017-02-17

Locations

1 site across 1 country: Canada