Evaluation of Surface Refractive Index Shift of Kalifilcon A Lenses Compared to Dailies Total 1, Precision 1 and Biotrue ONEday Lenses

Completed · Not applicable

Conditions studied: Habitual Soft Contact Lens Use

In brief

Approximately 20 habitual soft contact lens wearing participants will be enrolled in this unilateral, randomized, double-masked (participant and investigator masked) repeated measures insertion study. All participants will be seen for a Screening/Dispensing Visit at which informed consent will be obtained and eligibility will be assessed. If participants satisfy all eligibility criteria and none of the exclusion criteria, subjects will insert study lenses in random, successive order according to unique randomization schedules that will be provided to each Investigator.

Key facts

Study ID

NCT04555031

Run by

Bausch & Lomb Incorporated

People needed

10

Starts

2020-09-09

Expected to finish

2020-09-16

Last updated by the study team

2021-11-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older and have full legal capacity to volunteer.
• Physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings.
• No active ocular disease or allergic conjunctivitis.
• Not using any topical ocular medications.
• Willing and able to follow instructions.
• 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 and Lomb Site 01 — Rochester, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.