NCT07473557

Clinical Outcomes of the Use of a Femtosecond Laser on an Implanted Intraocular Lens

A Prospective Study to Assess the Clinical and Refractive Outcomes of the Use of a Femtosecond Laser on an Implanted Intraocular Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 12 (actual)
• Sponsor: Perfect Lens, LLC · Industry
• Sex: All
• Age: —
• Healthy volunteers: Accepted

Summary

This is a prospective non-randomized patient controlled single center study which is designed to evaluate the clinical outcomes of the treatment of an implanted intraocular lens using a low-energy femtosecond laser for refractive correction.

Detailed description

The purpose of this research study is to evaluate the safety and efficacy of the treatment of an implanted intraocular lens with a device. The device employs a generic femtosecond laser used in numerous other ophthalmic procedures. The device uses low levels of energy from the femtosecond laser to correct spherical, cylindrical and sphero-cylindrical refractive error existing in an implanted intraocular lens. The refractive correction is effected through the treatment, which is employed at least 30 days after cataract surgery.

Conditions

• Refractive Error Correction

Interventions

Type	Name	Description
OTHER	Device	The Perfector is used in the procedure. The device is attached to the patient by the use of a patient attachment. The patient attachment attaches to the sclera of the eye using vacuum pressure.

Timeline

• Start date: 2019-01-18
• Primary completion: 2022-09-16
• Completion: 2022-09-16
• First posted: 2026-03-16
• Last updated: 2026-03-19

Locations

1 site across 1 country: Panama