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Ocular Responses to Short and Long-term Lens Wear

NCT00722891 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2019-11-26

No results posted yet for this study

Summary

The purpose of this study was to determine whether ocular surface sensitivity to pneumatic, mechanical and chemical stimulation would be affected by the use of the combination of a specific silicone hydrogel lens material with two lens care products over a four week period.

Conditions

  • Ametropia

Interventions

DEVICE

Purevision Lenses with ReNu Multiplus

Purevision lenses using ReNu Multiplus lens solution for 28 days

DEVICE

Purevision Lenses with Optifree RepleniSH

Purevision lenses using Optifree RepleniSH lens solution for 28 days

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Trefford Simpson, DipOptom,MSc,PhD · University of Waterloo

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2009-06-30
Completion
2009-09-30

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 NCT00722891 on ClinicalTrials.gov