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

NCT02251561 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2015-06-10

Study results available
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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.

Conditions

  • Corneal Staining

Interventions

DEVICE

FID 109182

Investigational multipurpose contact lens cleaning and disinfecting solution

DEVICE

Opti-Free Plus

Commercially available multipurpose contact lens cleaning and disinfecting solution

DEVICE

Senofilcon A contact lens

Commercially available silicone hydrogel contact lens

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Tsunemitsu Senta · Alcon Japan, Ltd.

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2014-05-31
Completion
2014-05-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02251561 on ClinicalTrials.gov