Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Refractive Error
- Sponsor
- Alcon Research
- Enrollment
- 68
- Locations
- 1
- Primary Endpoint
- Overall Quality of Vision
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
The purpose of this study is to obtain on-eye performance data to inform contact lens product development and to further evaluate product performance in the intended population.
Detailed Description
The expected duration of subject participation in the study is approximately 20 days with 3 scheduled visits. Each subject will evaluate the test contact lenses compared to 1 of 3 commercially available contact lenses.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Able to understand and must sign an approved Informed Consent Form
- •Successfully wears daily disposable spherical soft contact lenses in both eyes for a minimum of 5 days per week and 8 hours per day during the past 3 months
- •Best Corrected Visual Acuity of 20/25 Snellen or better in each eye
- •Willing to stop wearing habitual contact lenses for the duration of study participation
- •Other protocol-defined inclusion criteria may apply
Exclusion Criteria
- •Any eye condition, surgery, disease, or use of medication that contraindicates contact lens wear, as determined by the Investigator.
- •Routinely sleeps in habitual contact lenses
- •Currently wears Oasys 1-Day, MyDay, or Moist contact lenses
- •Other protocol-defined exclusion criteria may apply
Outcomes
Primary Outcomes
Overall Quality of Vision
Time Frame: Day 8, each product
Overall quality of vision was collected binocularly and rated on a 10-point scale with 1 = poor to 10 = excellent. Subjects were asked "Thinking back over the last week, please rate our study lenses. Rate eyes together." No formal hypotheses was conducted; hence no inferential testing was performed.