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Comparison of Two Marketed Silicone Hydrogel Lenses

NCT02495948 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2016-12-28

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate cholesterol sorption by AIR OPTIX® AQUA lenses compared to ULTRA lenses after 30 days of wear.

Conditions

  • Refractive Error

Interventions

DEVICE

Lotrafilcon B contact lenses

DEVICE

Samfilcon A contact lenses

DEVICE

Hydrogen peroxide solution

Used as a cleaning, disinfection, and storage solution for silicone hydrogel and soft contact lenses

DEVICE

Saline solution

Used for rinsing contact lenses, as needed

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Manager, Vision Care, GCRA · Alcon, A Novartis Division

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2015-10-31
Completion
2015-10-31

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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 NCT02495948 on ClinicalTrials.gov