The goal of this clinical trial is to evaluate the comparative efficacy and safety of Hydrus Microstent, incisional goniotomy, and excisional goniotomy when combined with cataract surgery in patients with mild and moderate open-angle glaucoma. The main questions it aims to answer are: * How do the intraocular pressure lowering effects of these three microinvasive glaucoma surgeries compare? * How do the safety profiles of these three microinvasive glaucoma surgeries compare? Participants will be randomized to one of these three microinvasive glaucoma surgeries in combination with cataract surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
243
Patients will have a Hydrus Microstent inserted into the canal of Schlemm at the time of cataract surgery
Patients will have incisional goniotomy to open the trabecular meshwork with a Sinskey hook at the time of cataract surgery
Patients will have excisional goniotomy to remove the trabecular meshwork with a Kahook Dual Blade at the time of cataract surgery
Massachusetts Eye and Ear
Boston, Massachusetts, United States
RECRUITINGIntraocular pressure
Time frame: 3 years
Intraocular pressure-lowering medications
Time frame: 3 years
Surgical complications
Time frame: 3 years
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