keratoconus
Conditions
Interventions
Group 1: patients with healthy eyes
The study consists of one single examination: one measurement with the IOL Master 700 and one measurement with the Pentacam AXL.
Group 2: patients after refractive
Sponsors
Universitätsklinikum Frankfurt, Klinik für Augenheilkunde
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: healthy eyes, previous refractive surgery or keratoconus
Exclusion criteria
Exclusion criteria: Other ocular diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IOL decision with different professional experience in the two different corneal images | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the corneal images of the two devices regarding the IOL decision | — |
Countries
Germany
Contacts
Public ContactThomas Kohnen
Universitätsklinikum Frankfurt, Klinik für Augenheilkunde
Outcome results
None listed