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Intraocular Lens Implant Registry Study

ConditionsIntraocular Lens ComplicationIntraocular Lens RotationIntraocular Lens Associated Postoperative InflammationLens Opacities
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital Augsburg

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Patients who receive an intraocular lens are offered to participate in the study.

Trial design

Design model

Other

Time perspective

Other

Treatments tested in this trial

  • Intraocular lens Implantation

    Device

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

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Functional results with different Intraocular lenses

Visual acuity with different intraocular lenses is determined.

Time frame
6 months
2

Contrast sestivitiy with different Intraocular lenses

Contrast sensitivity with different intraocular lenses is determined.

Time frame
6 months
3

Anatomical results.

Anatomical results with different intraocular lenses are determined.

Time frame
6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital Augsburg

Lead sponsor

Source ClinicalTrials.gov
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