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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


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

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