H26.0 H26.1
Conditions
Interventions
Group 1: Cross-sectional check-up of recipients of bag-in-the-lens (BIL) intraocular lens implantation. Assessment includes: Refraction, best corrected visual acuity, intraocular pressure, biometry, c
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
1 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who have received phacoemulsification and intraocular lens implantation surgery since January 1, 2000 and who had not yet reached the age of 14 years at the time of surgery. At least 6 months must have passed between the time of surgery and the last examination.
Exclusion criteria
Exclusion criteria: Congenital Glaucoma Corneal Disease Microphthalmus (axis length < 17 mm) Anterior segment dysgenesis Other severe ocular or systemic malformation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time until relevant visual axis opacification in the operated eye | — |
Secondary
| Measure | Time frame |
|---|---|
| Time until peripheral visual axis opacification (without visual impairment) Influence of the type of intraocular lens (brand, model, material), influence of the biometric device used and the biometric formula, complications (especially secondary cataract, nystagmus, glaucoma, cystoid macular edema, detachment of the retina, eccentrically positioned IOL), characterization of the patient population (age, sex, relevant previous diseases and treatments, etc.), deviation from the target refraction, biometric error | — |
Countries
Germany
Contacts
Public ContactWolf Lagrèze
Universitätsklinikum Freiburg, Klinik Für Augenheilkunde, Sektion NKS
Outcome results
None listed