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For each eye in the study, 10 consecutive measurements were recorded for this field point.
Three NCT measurements, three ICare measurements and three GAT measurements were taken for each eye in the study.
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Table 1 shows the results for the 40 eyes included in the study.
No concomitant treatments for macular edema in the study eye were allowed during the study.
Donor eyes selected for research were logged in an eye tissue database for use in the study.
One randomly selected eye from each eligible healthy individual was chosen for inclusion in the study.
For glaucoma patients only the affected eye was included in the study.
Sixteen eyes of 8 patients were screened for inclusion in the study.
The right eye was designated the study eye in 206 (69.8%) patients.
If only 1 eye met the IOP criteria and was to receive study medication, that eye was appointed the study eye; if both eyes were to receive medication, the eye with the highest IOP at baseline (i.e., the second eligibility visit) was the study eye; and if baseline IOP was equal in both eyes, the right eye was designated as the study eye.
Ninety-two eyes were included in the study.
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