H52.1
Conditions
Interventions
Group 1: Myopia patients undergoing SMILE surgery
Group 2: Hyperopia patients receiving FEMTO-LASIK surgery
Sponsors
Experimental Eye research Institute Knappschaftskrankenhaus Bochum-Langendreer
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Myopia or hyperopia
Exclusion criteria
Exclusion criteria: systemic disease that contradicts surgery, as well as corneal abnormalities or diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in tear film parameters changes (cytokine changes, Schirmer test values) 3 months postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual acuity changes (visual acuity test) 3 months postoperatively | — |
Countries
Germany
Contacts
Public ContactSuphi Taneri
Zentrum für Refraktive Chirurgie Münster FranziskusCarré
Outcome results
None listed