A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD
This is a multicenter, controlled, randomized, monocular trial evaluating the safety and effectiveness of the Bausch \& Lomb DVisc40 dispersive OVD compared to the Alcon VISCOAT® dispersive OVD when used in cataract surgery. Subjects will be randomized to one of the two treatment groups in a 1:1 ratio (DVisc40:VISCOAT®).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
372
Ophthalmic viscosurgical device
Ophthalmic viscosurgical device
Valeant Site 01
San Diego, California, United States
Percent Change in Mean Epithelial Cell Density (ECD)
Time frame: Day 90
Percentage of Participants With Postoperative Intraocular Pressure of at Least 30 mm Hg
Time frame: 90 days
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