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Ocular Comfort and the "Aging" Lens (ERBIUM)

NCT01198600 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2012-08-29

Study results available
· View outcomes & findings →

Summary

The purpose of this trial was to evaluate the factors affecting comfortable contact lens wear and how those factors affect contact lens replacement frequency.

Conditions

  • Refractive Error

Interventions

DEVICE

Habitual contact lens

Hydrogel or silicone hydrogel contact lens per participant's habitual brand and prescription

DEVICE

Lotrafilcon B contact lens

Commercially marketed silicone hydrogel contact lens

DEVICE

Contact lens cleaning and disinfecting system (ClearCare)

Commercially marketed, hydrogen peroxide-based contact lens care system

Sponsors & Collaborators

  • University of Waterloo

    collaborator OTHER

  • CIBA VISION

    lead INDUSTRY

Principal Investigators

  • Desmond Fonn, MOptom FAAO · University of Waterloo Centre for Contact Lens Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2011-07-31
Completion
2011-07-31

Countries

  • Canada

Study Locations

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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 NCT01198600 on ClinicalTrials.gov