Condition: Visual Outcome · Sponsor: Hoya Surgical Optics, Inc.
This is a prospective, multicenter, parallel groups, non-interventional, examiner masked, comparative clinical study. Patients that participated in previous Hoya studies, and patients previous implanted with Hoya non-toric monofocal IOLs (sub-study only) will be enrolled in the study. The sample size for this study is based on demonstrating the non-inferiority of the mean distance-corrected intermediate visual acuity (DCIVA) in Group 1 (Site 1) compared with Group 2 (Site 2).
This description comes directly from the study's public registry record.
Srividhya Medical Monitor · +1-909-680-3900 · srividhya.vilupuru@hoya.com
Always discuss trial participation with your own doctor first.
| Peregrine Eye Laser Institute | Manila, Philippines | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07595432