Registry for optimizing intraocular lens implants in cataract surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry study aims to enhance the outcomes of intraocular lens implants used during cataract surgery. It will establish a database to collect and analyze data from patients treated with these implants, focusing on both retrospective and prospective evaluations. The study will track various parameters, including visual acuity, intraocular pressure, and complications, over a follow-up period of up to 10 years. By gathering comprehensive data, the study seeks to improve both anatomical and functional results associated with modern intraocular lens technologies.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Treatment with an intraocular lens implant 18 years of age or older Patient consent Full legal capacity

Exclusion Criteria:

Dementia Pregnancy Breastfeeding

Where it's running

• University Hospital Augsburg
  Augsburg, Germany Recruiting

Study contacts

• Study coordinator: Isabella Baur, MD
• Email: Isabella.Baur@uk-augsburg.de
• Phone: 0049821 400-2566

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.