H40.1
Conditions
Interventions
Group 1: 100 healthy subjects - This group consists of subjects without glaucoma and serves as a control group to study normal conditions of the trabecular meshwork (TM), Schlemm canal (SC) and adjace
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Presence of informed consent, a spherical equivalent < 3 Dpt, and no other ophthalmologic concomitant diseases
Exclusion criteria
Exclusion criteria: Non-consenting adults; persons in closed facilities / in prison
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Image quality of the OCT volume scans of the TM - evaluation of the clarity and accuracy of the images produced by the OCT devices. | — |
Secondary
| Measure | Time frame |
|---|---|
| Ability to visualize the Schlemm's canal (SC) and detect any narrowing in glaucoma - Evaluate the effectiveness of OCT technology in visualizing the SC and identifying changes associated with glaucoma. Comparison of the iridocorneal angle (ICA) between healthy subjects and glaucoma patients - Investigate for differences or specific characteristics that occur in glaucoma patients compared to healthy individuals. Detailed characterization of the TM and SC in vivo - using the knowledge gained from the OCT scans to develop a deeper understanding of the structure and function of these areas of the eye under both normal and pathological conditions. | — |
Countries
Germany
Contacts
Public ContactThomas Ach
Universitätsklinikum Bonn
Outcome results
None listed