Status:
COMPLETED
Pilot Clinical Performance of a Silicone Hydrogel Lens for Up to Six Nights of Extended Wear
Lead Sponsor:
Alcon Research
Conditions:
Refractive Errors
Myopia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn continuously for up to...
Detailed Description
Subjects will be randomized to wear the investigational contact lens in 1 eye and the commercially available contact lens in the other eye. Subjects will be expected to attend 3 scheduled study visits...
Eligibility Criteria
Inclusion
- Key
- Able to understand and sign an IRB/IEC approved Informed Consent form.
- Successful wear of spherical soft contact lenses in both eyes during the past 3 months for a minimum of 5 days/week and in an extended wear modality at least 1 night/week.
- Best corrected visual acuity of 20/25 or better in each eye.
- Other protocol-specified inclusion criteria may apply.
- Key
Exclusion
- Any condition, use of medications, or surgery that could contraindicate contact lens wear, as determined by the Investigator.
- Any habitual wear of Biofinity contact lenses.
- Pregnant or breast-feeding.
- Other protocol specified exclusion criteria may apply.
Key Trial Info
Start Date :
August 3 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 31 2020
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT04403542
Start Date
August 3 2020
End Date
August 31 2020
Last Update
August 22 2023
Active Locations (3)
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1
Alcon Investigator 6402
Medina, Minnesota, United States, 55340
2
Alcon Investigator 8046
Granville, Ohio, United States, 43023
3
Alcon Investigator 2786
Memphis, Tennessee, United States, 38119