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Clinical Trial Summary

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.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT04555031
Study type Interventional
Source Bausch & Lomb Incorporated
Status Completed
Phase N/A
Start date September 9, 2020
Completion date September 16, 2020

See also
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