Registry for optimizing intraocular lens implants in cataract surgery
Development of a Database to Optimize the Results With Intraocular Lens Implants
This study is collecting information from cataract surgery patients to see how well different types of lens implants work and to improve their outcomes over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital Augsburg Academic / other |
| Locations | 1 site (Augsburg) |
| Trial ID | NCT06294405 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are undergoing treatment with an intraocular lens implant.
Not a fit: Patients with dementia, those who are pregnant, or breastfeeding will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved visual outcomes and reduced complications for patients undergoing cataract surgery.
How similar studies have performed: Other studies have shown success in optimizing outcomes with intraocular lens implants, making this approach both relevant and promising.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Augsburg
- University Hospital Augsburg — Augsburg, Germany (Recruiting)
Study contacts
- Study coordinator: Isabella Baur, MD
- Email: Isabella.Baur@uk-augsburg.de
- Phone: 0049821 400-2566
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.