Clinical Evaluation of the Long-Term Effects of Contact Lens Care Systems

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study is to compare two marketed contact lens care solutions in regards to comfort and ocular health.

Key facts

Study ID

NCT00813761

Run by

Johnson & Johnson Vision Care, Inc.

People needed

473

Starts

2008-09-01

Expected to finish

2009-08-01

Last updated by the study team

2018-06-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be at least 18 years old.
• Signed Informed Consent and Investigator to record this on Case Report Form (CRF) in appropriate space.
• Require a visual correction in both eyes (monovision allowed but not monofit).
• Have a contact lens spherical distance requirement between +6.00D and -9.00D in both eyes.
• Astigmatism of 1.00D or less in the better eye and 1.50D or less in the other eye.
• Be correctable to a visual acuity of 20/30 (6/9) or better in each eye.
• Have normal eyes with no evidence of abnormality or disease.

You may not qualify if…

• Requires concurrent ocular medication.
• Any systemic illness which would contraindicate lens wear or the medical treatment of which would affect vision or successful lens wear.
• Clinically significant corneal edema, corneal vascularisation, tarsal abnormalities, bulbar injection or any other abnormality of the cornea that would contraindicate contact lens wear.
• Worn lenses on an extended wear basis in the last 3 months.
• Diabetic.
• Infectious disease (e.g., hepatitis, tuberculosis) or an immunosuppressive disease (e.g., HIV).
• Polymethyl methacrylate (PMMA) or rigid gas-permeable (RGP) lens wear in the previous 8 weeks.
• Has had refractive surgery. Has had eye injury/surgery within 8 weeks immediately prior to enrolment for this study.
• Abnormal lacrimal secretions.

Where it is running

• Study site — North Little Rock, Arkansas, United States
• Study site — Campbell, California, United States
• Study site — Cupertino, California, United States
• Study site — Laguna Niguel, California, United States
• Study site — Mission Viejo, California, United States
• Study site — San Clemente, California, United States
• Study site — Colorado Springs, Colorado, United States
• Study site — Bloomington, Illinois, United States
• Study site — Neodesha, Kansas, United States
• Study site — Raytown, Missouri, United States
• Study site — Warrensburg, Missouri, United States
• Study site — Florence, New Jersey, United States
• Study site — Chagrin Falls, Ohio, United States
• Study site — Warren, Ohio, United States
• Study site — Kittanning, Pennsylvania, United States
• Study site — Moon Township, Pennsylvania, United States
• Study site — Nanticoke, Pennsylvania, United States
• Study site — State College, Pennsylvania, United States
• Study site — Warwick, Rhode Island, United States
• Study site — Chamberlain, South Dakota, United States
• Study site — Bartlett, Tennessee, United States
• Study site — Salt Lake City, Utah, United States
• Study site — Burlington, Vermont, United States
• Study site — Midlothian, Virginia, United States
• Study site — Virginia Beach, Virginia, United States

Full record on ClinicalTrials.gov

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