Intraocular Lens Implant Registry Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Intraocular lens Implantation.
- Who it may be relevant to
- Registry conditions: Intraocular Lens Complication, Intraocular Lens Rotation, Intraocular Lens Associated Postoperative Inflammation, Lens Opacities. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Development of a Database to Optimize the Results With Intraocular Lens Implants
Overview
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
- Device Intraocular lens Implantation
Intraocular lenses are implanted during cataract surgery to replace the human crystalline lens.
Primary outcome measures
- Functional results with different Intraocular lenses [Time frame: 6 months]
- Contrast sestivitiy with different Intraocular lenses [Time frame: 6 months]
- Anatomical results. [Time frame: 6 months]
Eligibility 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Other
Study locations
Germany · 1 center
- University Hospital Augsburg — Augsburg
Identifiers
NCT: NCT06294405 · 24-0010