Intraocular Lens Implant Registry Study

Last updated: March 4, 2024
Sponsor: University Hospital Augsburg
Overall Status: Active - Recruiting

Phase

N/A

Condition

Inflammation

Eye Disorders/infections

Eye Disease

Treatment

Intraocular lens Implantation

Clinical Study ID

NCT06294405
24-0010
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

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

Eligibility Criteria

Inclusion

Inclusion Criteria: Treatment with an intraocular lens implant 18 years of age or older Patient consent Fulllegal capacity

Exclusion

Exclusion Criteria: Dementia Pregnancy Breastfeeding

Study Design

Total Participants: 500
Treatment Group(s): 1
Primary Treatment: Intraocular lens Implantation
Phase:
Study Start date:
February 21, 2024
Estimated Completion Date:
February 14, 2029

Study 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.

Connect with a study center

  • University Hospital Augsburg

    Augsburg,
    Germany

    Active - Recruiting

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