ClinicalTrials.gov
ClinicalTrials.gov Menu

Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
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

August 10, 2006
August 15, 2006
March 21, 2008
August 2006
Not Provided
Not Provided
Not Provided
Complete list of historical versions of study NCT00363623 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses
Not Provided
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.
Not Provided
Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single
Primary Purpose: Treatment
  • Myopia
  • Hyperopia
Device: Silicone hydrogel contact lens
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
44
Same as current
December 2006
Not Provided

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
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Australia
 
 
NCT00363623
H06 009
Not Provided
Not Provided
Not Provided
Not Provided
University of Melbourne
CIBA VISION
Principal Investigator: Carol Lakkis, BScOptom, PhD Clinical Vision Research Australia, University of Melbourne
University of Melbourne
February 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP