H18.5
Conditions
Interventions
Group 1: - visual acuity, measured by autorefraction and best corrected subjective visual acuity
- pachymetry measured by Pentacam (Oculus, Wetzlar, Germany)
- endothelial cell density (Topcon, Hambu
Sponsors
Augenklnik Universität Düsseldorf
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: The patients are able and willing to participate in the investigations required for the study.
Exclusion criteria
Exclusion criteria: Any physical disabilities which enable the patients to participate in the investigations.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - visual acuity, measured by autorefraction and best corrected subjective visual acuity - pachymetry measured by Pentacam (Oculus, Wetzlar, Germany) Both parameters are evaluated preoperatively and six weeks / six months postoperatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| endothelial cell density (Topcon, Hamburg, Germany) measured preoperatively and 6 weeks / six months postoperatively. | — |
Countries
Germany
Contacts
Public ContactKristina Spaniol
Universitätsaugenklinik Düsseldorf
Outcome results
None listed