NCT06294405

Intraocular Lens Implant Registry Study

Development of a Database to Optimize the Results With Intraocular Lens Implants

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 500 (estimated)
• Sponsor: University Hospital Augsburg · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

The goal of this registry study is to optimize the results with intraocular lens implants used in cataract surgery.

Detailed description

A variety of intraocular lens implants are available for patients undergoing cataract surgery and new technologies are continuously being developed in this field. In the planned monocentric retro- and prospective clinical study, a database to optimize outcomes with modern intraocular lens implants will be established to further improve anatomical and functional outcomes. Patients treated with an intraocular lens implant will be included. The retrospective evaluation of data includes data routinely collected prior to study inclusion (preoperative, intraoperative, postoperative up to the 1st study visit). Prospectively, refraction, visual acuity, examination findings, intraocular pressure and complications are recorded 1-6 months postoperatively. Depending on the type of IOL, results of further non-invasive measurements are also recorded. Optional follow-up visits with the aforementioned examinations are possible up to 10 years postoperatively.

Conditions

• Intraocular Lens Complication
• Intraocular Lens Rotation
• Intraocular Lens Associated Postoperative Inflammation
• Lens Opacities

Interventions

Type	Name	Description
DEVICE	Intraocular lens Implantation	Intraocular lenses are implanted during cataract surgery to replace the human crystalline lens.

Timeline

• Start date: 2024-02-21
• Primary completion: 2029-02-14
• Completion: 2029-02-14
• First posted: 2024-03-05
• Last updated: 2024-03-05

Locations

1 site across 1 country: Germany