Status:
COMPLETED
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Lead Sponsor:
Alcon Research
Conditions:
Refractive Error
Eligibility:
All Genders
18+ years
Phase:
NA
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 availab...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
January 10 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 16 2018
Estimated Enrollment :
68 Patients enrolled
Trial Details
Trial ID
NCT03349632
Start Date
January 10 2018
End Date
February 16 2018
Last Update
February 22 2019
Active Locations (3)
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1
Alcon Investigative Site
Maitland, Florida, United States, 32751
2
Alcon Investigative Site
Pensacola, Florida, United States, 32503
3
Alcon Investigative Site
Johns Creek, Georgia, United States, 30097