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Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear

NCT00346593 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2007-02-12

No results posted yet for this study

Summary

The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.

Conditions

  • Myopia

Interventions

DEVICE

Silicone hydrogel contact lens

Sponsors & Collaborators

  • Clinical Vision Research Australia

    collaborator OTHER

  • Cooper Companies

    collaborator INDUSTRY

  • University of Melbourne

    lead OTHER

Principal Investigators

  • Carol Lakkis, BScOptom PhD · Clinical Vision Research Australia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-05-31
Completion
2006-12-31

Countries

  • Australia

Study Locations

More Related Trials

Entities

Companies

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 NCT00346593 on ClinicalTrials.gov