H40.1 H18.5 H35.3 H25.9
Conditions
Interventions
Group 1: All 30 patients who are routinely operated on one of the 3 clinical standard indications (corneal, retina or glaucoma) are measured with both Sotware 1 and Software 2.
Because the two OCT sof
Sponsors
Universitätsaugenklinik
Eligibility
Sex/Gender
All
Age
21 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. The subject is = 21 years and mentally competent to fully understand the aim and conduct of the study 2. The subject has provided written informed consent 3. Subjects are undergoing a corneal, glaucoma and/or retinal surgery, planned independently of this study
Exclusion criteria
Exclusion criteria: 1. Patients who receive emergency surgical intervention 2. Ocular condition, which prevents the use of the RESCAN System 3. Patients unable to consent to participate in the clinical study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The image quality of the OCT images at scan depth 2.0 mm (Software 1) with those of 2.9 mm and 5.8 mm (Software 2) for the two RESCAN 700 systems is to be assessed. 2. Evaluation of the quality of distinctness of so-called ghost images and their influence on the interpretability of OCT images in 5.8 mm scan depth by 3 independent medical experts | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary endpoints. | — |
Countries
Germany
Contacts
Public ContactAngela Ehmer
Universitätsaugenklinik
Outcome results
None listed