The objective of this study is to evaluate the product performance of an investigational multifocal low add soft contact lens.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SCREENING
Masking
DOUBLE
Enrollment
126
Multifocal contact lens worn on a daily wear basis for 1 week
PureVision multifocal contact lens worn on a daily wear basis for 1 week.
Bausch & Lomb Incorporated
Rochester, New York, United States
Visual Acuity
Visual acuity was assessed by distance high contrast logarithm of the minimum angle of resolution (logMAR).
Time frame: At 1 week follow up
Symptoms/Complaints
Symptoms/complaints were assessed on a scale from 0 to 100, with 0 denoting unfavorable symptoms/complaints.
Time frame: At 1 week follow up
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