ORYOM Robotic Surgical System in Cataract Surgery
This is a prospective, open-label clinical study designed to evaluate the performance and safety of the ORYOM Robotic Surgical System during cataract surgery.
| Condition(s) | Cataract |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | This is a prospective, open-label clinical study designed to evaluate the performance and safety of the ORYOM Robotic Surgical System during cataract surgery. |
| Who can participate | Main Inclusion Criteria: * Patient aged 55 to 80 years * Willing and able to sign an informed consent, attend the clinic and comply with all study procedures and the study protocol * Patients are scheduled to undergo cataract surgery * Clear intraocular media, other than cataract * Pupil dilate according to stand of care Main Exclusion Criteria: * Prior ocular surgery or trauma in the study eye * Polar cataract in the study eye * Zonular instability or significant anterior segment abnormalities * Active ocular infection or uveitis * Pseudoexfoliation (PXF) syndrome in either eye * ASA Physical Status Classification \> 3 * Participation in another clinical trial within 30 days |
| Ages | 55 Years to 80 Years |
| Sex | All |
| Lead sponsor | ForSight Robotics Ltd |
| Locations | Makati City, National Capital Region, Philippines |
| Start date | 2026-02-20 |
| NCT ID | NCT07468409 |
| Official listing | https://clinicaltrials.gov/study/NCT07468409 |