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Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses

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ClinicalTrials.gov Identifier: NCT00363623
Recruitment Status : Completed
First Posted : August 15, 2006
Last Update Posted : March 21, 2008
Sponsor:
Collaborator:
CIBA VISION
Information provided by:
University of Melbourne

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
Myopia Hyperopia Device: Silicone hydrogel contact lens

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 44 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single
Primary Purpose: Treatment
Study Start Date : August 2006
Estimated Study Completion Date : December 2006

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Eye Wear
U.S. FDA Resources





Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00363623


Locations
Australia, Victoria
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

ClinicalTrials.gov Identifier: NCT00363623     History of Changes
Other Study ID Numbers: H06 009
First Posted: August 15, 2006    Key Record Dates
Last Update Posted: March 21, 2008
Last Verified: February 2007

Additional relevant MeSH terms:
Hyperopia
Refractive Errors
Eye Diseases