Intraocular Lens Implant Registry Study

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06294405

Enrollment

500

Registered

2024-03-05

Start date

2024-02-21

Completion date

2029-02-14

Last updated

2024-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

Interventions

DEVICEIntraocular lens Implantation

Intraocular lenses are implanted during cataract surgery to replace the human crystalline lens.

Study design

Observational model

OTHER

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

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

Exclusion criteria

Dementia Pregnancy Breastfeeding

Design outcomes

Primary

Measure	Time frame	Description
Functional results with different Intraocular lenses	6 months	Visual acuity with different intraocular lenses is determined.
Contrast sestivitiy with different Intraocular lenses	6 months	Contrast sensitivity with different intraocular lenses is determined.
Anatomical results.	6 months	Anatomical results with different intraocular lenses are determined.

Countries

Germany

Contacts

Primary ContactIsabella Baur, MD

Isabella.Baur@uk-augsburg.de0049821 400-2566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026