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Dispensing Overnight Study in Lenses

NCT00349856 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2009-02-18

No results posted yet for this study

Summary

The purpose of the study is to evaluate the fit and performance of an investigational soft contact lens in comparison with a currently marketed lens. Both lenses will be worn on a continuous wear basis, which means the lenses will be worn while sleeping.

Conditions

  • Myopia

Interventions

DEVICE

Biofinity

Soft contact lens

Sponsors & Collaborators

  • Cooper Companies

    collaborator INDUSTRY

  • University of Waterloo

    lead OTHER

Principal Investigators

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

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2005-01-31
Primary Completion
2008-03-31
Completion
2008-03-31

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 NCT00349856 on ClinicalTrials.gov