Pseudophakia
Conditions
Interventions
Group 1: All patients who have had a special lens implanted and whose last follow-up was at least six months ago are to be included. For this purpose, all former study participants will be contacted b
Sponsors
Universitätsklinikum Frankfurt, Klinik für Augenheilkunde
Eligibility
Sex/Gender
All
Age
30 Years to No maximum
Inclusion criteria
Inclusion criteria: - Pseudophakia - Patients aged 30 years and older - Treatment with an intraocular lens implanted in the capsular bag - Signed informed consent form, whereby the subjects have been informed in detail about the purpose of the study and participate voluntarily - Presence of preoperative data
Exclusion criteria
Exclusion criteria: - none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - postoperative visual acuity at distance, intermediate and near using ETDRS (Early Treatment of Diabetic Retinopathia Study) charts - Glistening rate (determined by slit lamp examination and using Pentacam and OCT imaging) | — |
Secondary
| Measure | Time frame |
|---|---|
| - PCO rate / Nd:YAG rate - Tomographic changes in the anterior segment of the eye (Pentacam AXL from Oculus) - Changes in the intraocular lens (rotation, decentration) - Defocus curve - Contrast vision (Pelli Robson charts, FrACT) - Patient satisfaction - Recording of ocular treatments and interventions after implantation of the intraocular lens | — |
Countries
Germany
Contacts
Public ContactThomas Kohnen
Universitätsklinikum Fraankfurt, Klinik für Augenheilkunde
Outcome results
None listed