Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems

NCT01699750 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2014-12-08

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate the lipid uptake, wetting characteristics, and visual performance of AIR OPTIX® AQUA and ACUVUE® OASYS® with HYDRACLEAR® contact lenses when used in conjunction with two contact lens care systems.

Conditions

  • Myopia
  • Astigmatism
  • Refractive Error

Interventions

DEVICE

Lotrafilcon B contact lenses

Silicone hydrogel contact lenses, Phase 2

DEVICE

Senofilcon A contact lenses

Silicone hydrogel contact lenses, Phase 2

DEVICE

OPTI-FREE® PUREMOIST® MPDS

Contact lens care system, Phase 2

DEVICE

BIOTRUE®

Contact lens care system, Phase 2

DEVICE

Balafilcon A contact lenses

Silicone hydrogel contact lenses worn for 30 days, Phase 1

DEVICE

ReNu® Multiplus®

Contact lens care system used for 30 days, Phase 1

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Jami Kern, PhD · Alcon Research

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2013-11-30
Completion
2013-11-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT01699750 on ClinicalTrials.gov