Dry Eye Clinical Trial
Official title:
The Effect of Lifitegrast On Refractive Accuracy And Symptoms In Dry Eye Patients Undergoing Cataract Surgery
To determine if Xiidra® lifitegrast plays a role in the refractive accuracy when administered to patients preoperatively who are scheduled for cataract surgery and have a tear break up time (TBUT) ≤ 10 seconds and central corneal staining as defined by the Oxford scale
This will be a 4-week multicenter investigator-initiated study, in which a maximum of 200
subjects will be enrolled.
As many as two thirds of patients undergoing cataract surgery have dry eye. Often this latter
condition is under treated i.e., any dry eye treatment such as artificial tears, that is
being pursued in not adequately controlling the visually significant ocular surface
disruption, and patient still have corneal staining or a reduced tear break-up time (TBUT).
The investigators hypothesize that lifitegrast administered at least 4-week prior to
pre-operative biometry measurements will improve both the quality of measurements used to
choose an intraocular lens implant for surgery and the symptoms of patients with this
combination of conditions. This finding would suggest that pre-treatment with lifitegrast can
improve both the accuracy of surgery and patient comfort.
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