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A Contralateral Dispensing Clinical Trial of Study Test Silicone Hydrogel Lens Against Enfilcon A Silicone Hydrogel Lens

Myopia Clinical Trial

Official title:
A Contralateral Dispensing Clinical Trial of Study Test Silicone Hydrogel Lens Against Enfilcon A Silicone Hydrogel Lens

Clinical Trial Summary

This will be a 1-month dispensing, double-masked, randomized, contralateral study comparing the test lens against the control lens. The assignment of lenses to eyes (i.e. which lens type is to be worn in which eye throughout the study) will be selected according to a randomization table.

Clinical Trial Description

Both test and control lenses will be used in a daily wear modality for 1 month. It is anticipated that this study will involve the following visits: Baseline (screening and dispense visit combined), 2-week visit and 4-week visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02537717
Study type Interventional
Source Coopervision, Inc.
Contact
Status Completed
Phase N/A
Start date October 1, 2015
Completion date April 29, 2016
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