Clinical Performance Comparison of Two Contact Lenses
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - 45 |
Updated: | 6/21/2018 |
Start Date: | August 1, 2009 |
End Date: | October 1, 2009 |
Clinical Evaluation of Two Silicone Hydrogel Frequent Replacement Contact Lenses
The purpose of this study is to compare the clinical performance of two contact lenses.
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
We found this trial at
24
sites
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