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Corneal and Conjunctival Sensitivity and Staining Study

NCT00455455 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2010-07-12

Study results available
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Summary

The primary objective of this study is to compare subjective symptoms and ocular health in a group of individuals who are currently wearing soft contact lenses on a daily wear basis, after a short period of no lens wear and during the time course when using differing care regimens.

Conditions

  • Myopia
  • Hyperopia

Interventions

DRUG

Optifree RepleniSH Multipurpose Disinfecting Solution

lens care system

DRUG

ReNu Multiplus Multipurpose Solution

lens care system

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • University of Waterloo

    lead OTHER

Principal Investigators

  • Desmond Fonn, M.Optom · University of Waterloo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-31
Primary Completion
2008-12-31
Completion
2008-12-31

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 NCT00455455 on ClinicalTrials.gov