MedTrace Logo

Clinical Performance of Extended Wear Silicone Hydrogel Lenses

NCT00441233 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2008-01-09

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 over a period of 6 months of extended wear.

Conditions

  • Myopia

Interventions

DEVICE

Silicone hydrogel contact lens

Sponsors & Collaborators

  • Menicon Co., Ltd.

    collaborator INDUSTRY

  • Clinical Vision Research Australia

    collaborator OTHER

  • University of Melbourne

    lead OTHER

Principal Investigators

  • Carol Lakkis, BScOptom, PhD, PGCertOcTher · Clinical Vision Research Australia, University of Melbourne

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2007-03-31
Primary Completion
2007-11-30
Completion
2007-12-31

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 NCT00441233 on ClinicalTrials.gov