Status:
COMPLETED
Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2
Lead Sponsor:
Alcon Research
Conditions:
Refractive Errors
Myopia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Clariti 1-Day contact lenses.
Detailed Description
Subjects are expected to attend 3 study visits and wear the PRECISION1 and Clariti 1-Day study lenses in a crossover design for approximately 8 days of exposure to each study lens type. The expected d...
Eligibility Criteria
Inclusion
- Key Inclusion Criteria
- Subject must be able to understand and must sign an Institution Review Board (IRB) approved Informed Consent Form.
- Successful wear of soft contact lenses in both eyes for a minimum of 5 days per week and 10 hours per day during the past 3 months.
- Willing to wear contact lenses for at least 16 hours per day on one of the days with each lens type.
- Other protocol-specified inclusion criteria may apply.
- Key Exclusion Criteria:
- Any ocular condition that contraindicates contact lens wear.
- Previous or current habitual wearer of PRECISION1, Clariti 1-Day, or DAILIES TOTAL1 contact lenses.
- Other protocol-specified exclusion criteria may apply.
Exclusion
Key Trial Info
Start Date :
September 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 16 2020
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT04528017
Start Date
September 1 2020
End Date
October 16 2020
Last Update
November 11 2021
Active Locations (4)
Enter a location and click search to find clinical trials sorted by distance.
1
Alcon Investigator 6565
Maitland, Florida, United States, 32751
2
Alcon Investigator 6402
Medina, Minnesota, United States, 55340
3
Alcon Investigator 6313
Powell, Ohio, United States, 43065
4
Alcon Investigator 8028
Wichita Falls, Texas, United States, 76308