NCT07276217

Phacoemulsification and Intraocular Lens Implantation: Patient Registry

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 300 (estimated)
• Sponsor: Sensor Cliniq · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The aim of the study is to create a patient registry that will allow for comparison of cataract treatment outcomes using phacoemulsification with implantation of different types of intraocular lenses.

Detailed description

This study will establish a registry to evaluate outcomes associated with intraocular lens implants in patients undergoing cataract surgery. Retrospective assessments will include routinely collected preoperative, intraoperative, and postoperative data. Prospectively, visual acuity, refraction, examination findings, patient-reported outcomes, and complications will be collected for up to 60 months after surgery.

Conditions

• Cataract
• Intraocular Lens

Interventions

Type	Name	Description
DEVICE	Intraocular lens	Implantation of an intraocular lens following phacoemulsification cataract extraction, with lens type selected according to routine clinical practice (e.g., monofocal, toric, multifocal, or extended-depth-of-focus).

Timeline

• Start date: 2025-01-02
• Primary completion: 2026-07-01
• Completion: 2026-07-01
• First posted: 2025-12-10
• Last updated: 2025-12-10

Locations

1 site across 1 country: Poland