Status:
COMPLETED
Performance Assessment of a Modified Daily Disposable Contact Lens
Lead Sponsor:
Alcon Research
Conditions:
Refractive Errors
Myopia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to compare visual acuity between two daily disposable contact lenses.
Detailed Description
The expected duration of subject participation in the study is approximately 2 weeks, with 3 scheduled visits.
Eligibility Criteria
Inclusion
- Able to understand and sign an approved Informed Consent form;
- Current wearer of commercial DAILIES TOTAL1 Contact Lenses in both eyes;
- Other protocol-specified inclusion criteria may apply.
Exclusion
- Any eye condition that contraindicates contact lens wear, as determined by the Investigator;
- Any eye surgery that contraindicates contact lens wear, as determined by the Investigator;
- Wears habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week)
- Monocular (only one eye with functional vision);
- Other protocol-specified exclusion criteria may apply.
Key Trial Info
Start Date :
December 3 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 7 2019
Estimated Enrollment :
62 Patients enrolled
Trial Details
Trial ID
NCT03762668
Start Date
December 3 2018
End Date
January 7 2019
Last Update
January 13 2020
Active Locations (5)
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1
Alcon Investigative Site
Maitland, Florida, United States, 32751
2
Alcon Investigative Site
Orlando, Florida, United States, 32803
3
Alcon Investigative Site
West Palm Beach, Florida, United States, 33405
4
Alcon Investigative Site
Ann Arbor, Michigan, United States, 48105