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Effectiveness of a Marketed One-Step Peroxide Lens Care Solution in Symptomatic Contact Lens Wearers

NCT01996709 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 142

Last updated 2015-06-08

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to assess improvement of palpebral roughness and associated symptoms with 3 months use of Clear Care®.

Conditions

  • Refractive Error

Interventions

DEVICE

Hydrogen peroxide-based contact lens solution

DEVICE

Habitual contact lens solution

Biguanide-preserved

DEVICE

Habitual contact lenses

Silicone hydrogel contact lenses with a biweekly or monthly replacement schedule

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Lisa Zoota, MPH · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
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 NCT01996709 on ClinicalTrials.gov