H25.1 T85.2 H26.4
Conditions
Interventions
Group 1: Patients who have undergone monocular or binocular ophthalmic implantation are prospectively revisited at 3 months to 10 years to assess visual acuity, refraction, and visual quality. The pre
Sponsors
International Vision Correction Research Centre (IVCRC), UNiversitäts-Augenklinik Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Condition following monocular or binocular fitting with an ophthalmic implant, female and male > 18 years, written informed consent, legal capacity
Exclusion criteria
Exclusion criteria: Dementia, pregnancy and lactation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Deviation target vs. achieved postoperative refraction (for IOL constant optimization) after 3 month only | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional results (refraction, visual acuity), subjective Patient satisfaction, Quality of Vision (contrast, spherical Aberration), stability of postoperative achieved results Preoperative data is evaluated retrospectively from pseudonymisiced patient files. The patients will be rescheduled for all examinations after 3 month, 1 year and 3 years. Patient satisfaction will be evaluated by self developed subjective questionaire | — |
Countries
Germany
Contacts
Public ContactRaquel Willrich
International Vision Correction and Research Centre (IVCRC), Universitäts-Augenklinik Heidelberg
Outcome results
None listed