Insertion Clinical Study to Evaluate the Aberration Characteristics of Kalifilcon A Toric Lenses

Completed · Not applicable

Conditions studied: Contact Lens Wearer

In brief

This objective of this clinical study aims to confirm whether multiple kalifilcon A daily disposable toric contact lenses are providing the intended level of spherical aberration correction when worn.

Key facts

Study ID

NCT05129072

Run by

Bausch & Lomb Incorporated

People needed

75

Starts

2021-08-25

Expected to finish

2021-09-24

Last updated by the study team

2025-06-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not 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.
• A women of childbearing potential (those who are not surgically sterilized or postmenopausal) are excluded from participation in the investigation if they meet any one of the following conditions: she is currently pregnant, she plans to become pregnant during the study, she is breastfeeding.

Where it is running

• Bausch and Lomb Site 01 — Rochester, New York, United States

Full record on ClinicalTrials.gov

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