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NCT Number: NCT06294405

Intraocular Lens Implant Registry Study

The goal of this registry study is to optimize the results with intraocular lens implants used in cataract surgery.

Recruiting

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Key information

Conditions

Intraocular Lens Complication Cataract Eye Diseases Intraocular Lens Associated Postoperative Inflammation Intraocular Lens Rotation Lens Diseases Lens Opacities

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Augsburg

Augsburg, Germany

Location status: Recruiting

Location contact

Isabella Baur, MD

CONTACT

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

Dementia Pregnancy Breastfeeding

Treatment and study plan

Intraocular Lens Implantation

Device

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

Primary outcomes

  1. Functional results with different Intraocular lenses

    Time frame: 6 months

    Visual acuity with different intraocular lenses is determined.

  2. Contrast sestivitiy with different Intraocular lenses

    Time frame: 6 months

    Contrast sensitivity with different intraocular lenses is determined.

  3. Anatomical results.

    Time frame: 6 months

    Anatomical results with different intraocular lenses are determined.

Study contacts

Contact information is provided by the study sponsor or research team.

Isabella Baur, MD

CONTACT

[email protected]

0049821 400-2566

Sponsors and collaborators

Lead sponsor

University Hospital Augsburg

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Mar 5, 2024
Registry last updated
Mar 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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