H25.8
Conditions
Interventions
Group 1: With optical coherence tomography (OCT), the center of the lens capsule is preoperatively determined.
Postoperatively, the measurement is repeated and the position of the intraocular lens is
Sponsors
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH Augenklinik
Eligibility
Sex/Gender
All
Age
22 Years to No maximum
Inclusion criteria
Inclusion criteria: • Visus-limiting lens restraints (Grade 1 - 5 / LOCS III classification) • Cataract-dependent visual performance of 0.8 or less • Patient age> 22 years • Planned surgery on the cataract in one eye • Understood and signed consent
Exclusion criteria
Exclusion criteria: • Previous corneal procedures or intraocular procedures • Pronounced (> 5 Dpt.) Or irregular corneal curvatures • active inflammation of the anterior or posterior eye segment • Z.n. ocular trauma • Pseudoexfoliation Syndrome • pre-existing or intraoperative zonularis • intraoperative capsule defects • Pupil width in mydriasis less than 6 mm • ash length less than 20.5 mm or greater than 25 mm • uncontrolled glaucoma • Congenital cataract • Pregnancy, planned pregnancy or nursing • Participation in a study in the last 30 days
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| • Correlation of the preoperatively measured capsule bag equatorial position (center of the capsule bag) with the postoperative position of the intraocular lens (center point of the IOL). • Comparison between capsule and forehead depth measurements Data collection using optical coherence tomography | — |
Secondary
| Measure | Time frame |
|---|---|
| • Determination of corrected and uncorrected visual acuity (refraction) pre- and postoperatively, with Standard method (projector). • Descriptive analysis of patients who can not be measured with the OCT | — |
Countries
Germany
Contacts
Public ContactTim Schultz
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH
Outcome results
None listed