H25.8 H52.2
Conditions
Interventions
Group 1: Standard cataract surgery with Implantation of the Toric Intraocular Lens Ancoris into one eye.
Sponsors
PhysIOL SALiège Science Park
Eligibility
Sex/Gender
All
Age
50 Years to No maximum
Inclusion criteria
Inclusion criteria: •Cataracteous Eyes with no comorbidity •Regular corneal astigmatism >1 dioptre and 50 years old
Exclusion criteria
Exclusion criteria: •Acute or chronic disease or illness that would increase risk or confound study results (e.g. diabetes mellitus (with retinopathy), immunocompromised, glaucoma etc…) •Any ocular comorbidity •History of ocular trauma or prior ocular surgery including refractive procedures •Capsule or zonular abnormalities that may affect postoperative centration or tilt of the lens (e.g. pseudoexfoliation syndrome, Marfan’s syndrome) •Pupil abnormalitis (non-reactive, tonic pupils, abnormally shaped pupils or pupils that do not dilate under mesopic/scotopic conditions)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determining the rotational stability of the intraocular lens (Ankoris) by photography of the IOL to the visits day 1, month 1 and month 3 with electronic measurement of the axial position. | — |
Secondary
| Measure | Time frame |
|---|---|
| Measuring the remaining astigmatism after Ankoris implantation compared to the target astigmatism by standard method (refraction) to the visits month 1 and month 3 | — |
Countries
Germany
Contacts
Public ContactTim Schultz
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH
Outcome results
None listed