The purpose of this study is to evaluate whether the TUG device is safe and effective in patients with primary open angle glaucoma or ocular hypertension.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
25
Change in mean IOP
Time frame: through subject study completion; average 2 months
Change in mean diurnal IOP
Time frame: Week 4 (Visit 5) and Week 8 (Visit 7)
Change in IOP from baseline
Time frame: through subject study completion; average 2 months
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