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Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in Japan

Corneal Staining Clinical Trial

Official title:
Clinical Evaluation of Opti-Free III Compared to Opti-Free Plus®

Clinical Trial Summary

The purpose of this study is to compare an investigational contact lens care product (FID 109182) to a commercially available contact lens product (Opti-Free Plus®) for corneal staining when used with Acuvue® Oasys® contact lenses. The contact lenses will be pre-soaked in the products for 24-48 hours prior to a 2-hour contralateral wear period.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02251561
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date May 2014
View Details
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