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Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses

Sponsor
University of Melbourne (Other)
Overall Status
Completed
CT.gov ID
NCT00363623
Collaborator
CIBA VISION (Industry)
44
Enrollment
1
Location
4
Duration (Months)
11
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The primary purpose of this study is to investigate the performance of contact lens maintenance systems when used with silicone hydrogel contact lenses during daily wear over a period of 1 month.

Condition or Disease Intervention/Treatment Phase
  • Device: Silicone hydrogel contact lens
 N/A

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single
Primary Purpose:
Treatment
Study Start Date :
Aug 1, 2006
Study Completion Date :
Dec 1, 2006

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Is correctable to at least 20/40 distance visual acuity in each eye with spherical contact lenses.

    • Is an experienced soft contact lens wearer for at least 1 month.

    • Has no clinically significant anterior eye findings.

    • Has no other active ocular disease.

    Exclusion Criteria:

    • Requires concurrent ocular medication.

    • Eye surgery or injury within 12 weeks prior to enrolment.

    • Has any systemic disease or ocular abnormality that might interfere with contact lens wear

    • Has any pre-existing ocular irritation that would preclude contact lens fitting.

    • PMMA lens wear previous 6 months.

    • EW or CW in previous 1 month.

    • Hydrogen peroxide users

    • Latex sensitivity

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Clinical Vision Research Australia Carlton Victoria Australia 3053

    Sponsors and Collaborators

    • University of Melbourne
    • CIBA VISION

    Investigators

    • Principal Investigator: Carol Lakkis, BScOptom, PhD, Clinical Vision Research Australia, University of Melbourne

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00363623
    Other Study ID Numbers:
    • H06 009
    First Posted:
    Aug 15, 2006
    Last Update Posted:
    Mar 21, 2008
    Last Verified:
    Feb 1, 2007
    Additional relevant MeSH terms:
    Hyperopia

    Study Results

    No Results Posted as of Mar 21, 2008