H40.1
Conditions
Interventions
Group 1: Patients in whom a daily tension profile is carried out under inpatient conditions to evaluate the therapeutic effect.
The intraocular pressure should be measured every 3 hours for 3 days. T
Sponsors
Dietrich-Bonhoeffer-KlinikumKlinik für Augenheilkunde
Eligibility
Sex/Gender
All
Age
21 Years to 85 Years
Inclusion criteria
Inclusion criteria: -Patients older than 21 years Patients' willingness to participate in the study and written informed consent. -Diagnosis of primary chronic open-angle glaucoma, pseudoexfoliation glaucoma, ocular hypertension requiring treatment or pigment dispersion glaucoma
Exclusion criteria
Exclusion criteria: Patients with poor general condition or poor compliance -Patients diagnosed with various eye disorders affecting the macular area -Patients with an acute angle-closure situation -Intravenous or oral ingestion of acetazolamide and/or mannitol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determination on the effect of the short-term effect of the eye drop application after 30 minutes and after 60 minutes on vessel density, area, circumference, circular shape of the foveal avascular zone using angio-OCT images | — |
Secondary
| Measure | Time frame |
|---|---|
| Long-term effect (permanently minimized FAZ) of local anti-glaucomatous therapy on patients who needed a renewed tension profile after 6/12 months | — |
Countries
Germany
Contacts
Public ContactUlrike Holland
Dietrich-Bonhoeffer-Klinikum, Klinik für Augenheilkunde
Outcome results
None listed