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Investigation of Multi-Purpose Solution-Based Corneal Staining and Ocular Comfort

NCT00349843 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-12-16

No results posted yet for this study

Summary

The primary objective of this study is to compare subjective ocular symptoms and corneal staining over time in a group of individuals who wear soft contact lenses on a daily wear basis, whilst they sequentially use two different contact lens care regimens.

Conditions

  • Myopia

Interventions

DEVICE

Soft contact lens

DRUG

Marketed soft lens multipurpose disinfection regimen

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • University of Waterloo

    lead OTHER

Principal Investigators

  • Craig Woods, PhD · University of Waterloo

  • Desmond Fonn, MOptom · University of Waterloo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-06-30

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 NCT00349843 on ClinicalTrials.gov