Kalifilcon A Toric Compared to Commercially Available Lenses

Completed · Not applicable

Conditions studied: Astigmatism

In brief

Approximately thirty contact lens adapted subjects will be enrolled in this feasibility, bilateral, randomized, double masked (subject and investigator masked), repeated measures insertion study.

Key facts

Study ID

NCT06098937

Run by

Bausch & Lomb Incorporated

People needed

30

Starts

2023-09-05

Expected to finish

2023-09-27

Last updated by the study team

2024-12-10

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 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 in the opinion of the Investigator.
• Considered by the Investigator to not be a suitable candidate for participation

Where it is running

• Bausch & Lomb, Incorporated — Rochester, New York, United States

Full record on ClinicalTrials.gov

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