Clinical Performance Comparison of Two Contact Lenses

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study is to compare the clinical performance of two contact lenses.

Key facts

Study ID

NCT00975585

Run by

Johnson & Johnson Vision Care, Inc.

People needed

379

Starts

2009-08-01

Expected to finish

2009-10-01

Last updated by the study team

2018-06-19

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Existing daily soft lens wearer.
• Require a distance visual correction in both eyes.
• Have a contact lens spherical distance refraction between -1.00D and -6.00D.
• Have refractive astigmatism less than or equal to 1.00D in both eyes.
• Achieve 20/30 or better corrected distance acuity.
• Have normal eyes with no evidence of abnormality or disease.

You may not qualify if…

• Requires presbyopic correction.
• Requires ocular medications.
• Grade 3 or 4 ocular abnormalities.
• Grade 3 corneal staining in more than one region.
• Has had refractive surgery.
• Any other injury or ocular surgery within 8 weeks prior to study enrollment.
• Has abnormal lacrimal secretions.
• Pre-existing ocular irritation that would preclude contact lens fitting.
• Has keratoconus or other corneal irregularity.
• Polymethyl methacrylate (PMMA), Hybrid or Rigid Gas Permeable (RGP) wear in the previous 8 weeks.
• Wears habitual contact lenses that are toric, multifocal or worn extended wear.
• Any systemic illness which would contraindicate lens wear or the medical treatment of would affect vision or successful lens wear.
• Diabetic.
• Infectious or immunosuppressive disease.
• History of chronic eye disease (e.g glaucoma or age related macular degeneration).
• Pregnancy, lactation or planning pregnancy at time of enrollment.
• Participation in any concurrent clinical trial or in another trial in the last 30 days.

Where it is running

• Study site — North Little Rock, Arkansas, United States
• Study site — Campbell, California, United States
• Study site — Colorado Springs, Colorado, United States
• Study site — Jacksonville, Florida, United States
• Study site — Jacksonville, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Winter Park, Florida, United States
• Study site — Roswell, Georgia, United States
• Study site — Boston, Massachusetts, United States
• Study site — Cambridge, Massachusetts, United States
• Study site — Blue Springs, Missouri, United States
• Study site — New York, New York, United States
• Study site — Chagrin Falls, Ohio, United States
• Study site — North Olmsted, Ohio, United States
• Study site — Warren, Ohio, 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 — Hot Springs, South Dakota, United States
• Study site — Bartlett, Tennessee, United States
• Study site — Brentwood, Tennessee, United States
• Study site — Memphis, Tennessee, United States
• Study site — Tyler, Texas, United States
• Study site — Burlington, Vermont, United States
• Study site — West Allis, Wisconsin, United States

Full record on ClinicalTrials.gov

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