RecruitingOBSERVATIONAL

Intraocular Lens Implant Registry Study

This research study is looking into intraocular lens (IOL) implants, which are special lenses used in cataract surgery. The main goal is to make sure these lens implants give the best possible results for patients, improving their vision and preventing potential problems after surgery. Researchers will collect information from patients who have received these implants. They'll look at existing records and also follow up with patients after their surgery to see how their vision is, if they have any complications, and how well the new lens is working. This information will then be used to understand how to make these treatments even better for future patients.

At a glance

Status

Recruiting

Sponsor

University Hospital Augsburg

Enrolment target

500

Start

21 Feb 2024

Estimated completion

14 Feb 2029

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

What is this study about?

This research is looking at special lenses called intraocular lens implants, or IOLs. These are artificial lenses that are put into your eye during cataract surgery to replace your cloudy natural lens, helping you to see clearly again. There are many different types of these lenses available, and new ones are always being developed.

The main aim of this study is to gather information to help make sure that these modern lens implants give the best possible results for people having cataract surgery. By collecting detailed information from patients, the researchers hope to better understand how different lenses perform. This includes looking at things like how sharp your vision becomes, whether you experience any problems or discomfort, and how the lens settles in your eye.

Ultimately, the goal is to use this gathered knowledge to improve how these lens implants work in the future. This means aiming for even better vision outcomes and fewer potential complications for everyone who undergoes cataract surgery.

Key takeaways

The study helps improve cataract surgery lens implants.
It collects information on how well lenses work and prevents problems.
Participation involves routine eye checks after surgery.
The study focuses on enhancing future patient outcomes.
You can stop participating at any point.

Who may be eligible?

To be part of this study, you must have received an intraocular lens implant as part of your cataract surgery. You also need to be at least 18 years old and capable of giving your full permission to be involved.

There are certain reasons why you wouldn't be able to join. These include if you have dementia, or if you are pregnant or breastfeeding. The study is open to both men and women.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

Have you had an intraocular lens implant?
Are you 18 years old or older?
Are you able to provide your own consent?
Are you not currently pregnant or breastfeeding?
Do you not have dementia?

Answer every question to see your result.

What does participation involve?

If you take part in this study, the researchers will look at information already collected from your routine check-ups before, during, and right after your lens implant surgery. After your surgery, you will have specific study visits to check your eyes. These visits will typically be between 1 and 6 months after your operation.

During these follow-up visits, doctors will measure your eyesight, check the pressure inside your eye, and examine how your new lens is doing. They will also note down any problems or complications you might experience. Depending on the type of lens you have, they might also carry out other non-invasive eye tests. Some participants might have the option for further follow-up visits for up to 10 years, though this is not required for everyone.

Potential risks and benefits

By taking part, you could be contributing valuable information that helps doctors better understand and improve lens implants for future patients. There are no direct medical benefits to you, as this study mainly involves collecting information from standard checks. As with any clinical study, you can choose to stop participating at any time without affecting your medical care.

Locations (1)

University Hospital Augsburg
Verified postcode
Augsburg, Germany· Recruiting

Common questions

What is an intraocular lens implant?

It's an artificial lens placed in your eye during cataract surgery to replace your cloudy natural lens and restore clear vision.

Why is this study being done?

The study aims to gather information to improve how well different lens implants work for patients after cataract surgery.

Will I have to take any new medicine?

No, this study does not involve taking any new medications. It's about observing the effects of your existing lens implant.

How long will I be involved in the study?

Regular study visits will happen 1 to 6 months after your surgery, with optional longer follow-ups for some people up to 10 years.

Will this study affect my standard medical care?

No, participating in this study will not change the standard medical care you receive for your eyes.

How to find out more

Isabella Baur, MD

isabella.baur@uk-augsburg.de 0049821 400-2566 Official trial record

Always speak to your GP or specialist before deciding to take part in a study.