NCT07447622

Clinical Outcomes of the Use of a Femtosecond Laser Treatment in a Patient With Implanted Monofocal IOLs

Assessment of Clinical and Refractive Outcomes of the Use of a Femtosecond Laser to Create Near Vision or Correct Refractive Error in a Patient With Implanted Monofocal IOLs

• Status: Not Yet Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 12 (estimated)
• Sponsor: Perfect Lens, LLC · Industry
• Sex: All
• Age: —
• Healthy volunteers: Accepted

Summary

This study aims to assess the safety and efficacy of evaluating near vision or refractive error in eyes implanted with a mono focal intraocular lens (IOL) using a low-energy femtosecond laser.

Detailed description

An investigative device built by Perfect Lens will be used to adjust an implanted intraocular lens (IOL). The device uses a femtosecond laser, a scanner, and an OCT. Each participant either does not have near vision or has refractive error pre-treatment. The primary endpoint for the treatment is to create near vision in the treated eye without sacrificing the existing far vision, or correct refractive error. The participants will be examined at 7 days, 30 days and 90 days after treatment.

Conditions

• Near Vision
• Refractive Error Correction

Interventions

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

Timeline

• Start date: 2026-03-01
• Primary completion: 2026-07-01
• Completion: 2026-09-01
• First posted: 2026-03-03
• Last updated: 2026-03-03

Locations

1 site across 1 country: Czechia