Intraocular Lens Implant Registry Study

Status Recruiting

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

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

Clinical Trial Details

NCT number	NCT06294405
Study type	Observational [Patient Registry]
Source	University Hospital Augsburg
Contact	Isabella Baur, MD
Phone	0049821 400-2566
Email	Isabella.Baur@uk-augsburg.de
Status	Recruiting
Phase
Start date	February 21, 2024
Completion date	February 14, 2029

View Details

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