1-Week Dispensing Evaluation of Kalifilcon A Toric Contact Lenses Compared to Ultra for Astigmatism

Completed · Not applicable

Conditions studied: Myopia, Astigmatism

In brief

Experienced soft contact lens wearing subjects will be enrolled in this 1-week, confirmatory, randomized, bilateral, 2-way crossover, double masked (subject and investigator), repeated measures, dispensing study. All subjects will be seen for a Screening/Baseline Visit at which informed consent will be obtained and eligibility will be assessed.

Key facts

Study ID

NCT05320042

Run by

Bausch & Lomb Incorporated

People needed

28

Starts

2022-02-14

Expected to finish

2022-05-10

Last updated by the study team

2022-11-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Be 18 years or older on the date the Informed Consent Form (ICF) is signed and have the capacity to read, understand and provide written voluntary informed consent.
• Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings.
• Have no active ocular disease or allergic conjunctivitis.
• Not be using any topical ocular medications.
• Be willing and able to follow instructions.
• Have signed a statement of informed consent.

You may not qualify if…

• Participating in a conflicting study.
• Considered by the Investigator to not be a suitable candidate for participation.

Where it is running

• Bausch site 1 — Rochester, New York, United States

Full record on ClinicalTrials.gov

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