RecruitingNot ApplicableNCT07468409
ORYOM Robotic Surgical System in Cataract Surgery
Single-site, Open-label, Prospective Feasibility Study Performed Using the ORYOM™ Robotic Surgical System in Cataract Surgery Procedures
Sponsor
ForSight Robotics Ltd
Enrollment
20 participants
Start Date
Feb 20, 2026
Study Type
INTERVENTIONAL
Conditions
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.
Eligibility
Min Age: 55 YearsMax Age: 80 Years
Inclusion Criteria5
- 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
Exclusion Criteria7
- 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
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Interventions
DEVICEORYOM™ Robotic Surgical System
The ORYOM Robotic Surgical System is a robotically assisted surgical system intended to assist ophthalmic surgeons in performing cataract surgery.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07468409
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