H26.9 H26
Conditions
Interventions
Group 1: First: Measurement of the refractive power of the intraocular lens (IOL) in the operating room with into the anterior chamber of the eye injected balanced salt solution.
Then: measuring the r
Sponsors
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH Augenklinik
Eligibility
Sex/Gender
All
Age
22 Years to No maximum
Inclusion criteria
Inclusion criteria: • lens opacities (Grade 1 - 5 / LOCS III classification) • cataract-related visual acuity of 0.8 or less • Patients aged> 22 years • Planned surgery on cataracts in one eye • Understood and signed informed consent
Exclusion criteria
Exclusion criteria: • Previous corneal surgery or intraocular surgery • High (> 5 Dpt.) Or irregular astigmatism • active inflammation of the anterior or posterior segment of the eye • Z.n. ocular trauma • Pseudoexfoliation • Pre-existing or intraoperative Zonulyse • intraoperative capsular defects • pupil size in mydriasis less than 6 mm • ash length is less than 20.5 mm, or greater than 25 mm • uncontrolled glaucoma • Congenital cataracts • pregnancy, planned pregnancy or breastfeeding • participate in a study in the last 30 days
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of intraoperatively determined IOL power with an intraoperative aberrometer after filling the anterior chamber with balanced salt solution or with a Viscoelastikum. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of pre- and intraoperatively calculated power with the achieved after 6 weeks postoperative results with standrad visual acuity testing | — |
Countries
Germany
Contacts
Public ContactTim Schultz
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH
Outcome results
None listed