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Clinical Trial Summary

To assure the quality of follow-up and treatment, data of glaucoma patients are stored and evaluated after anonymisation.


Clinical Trial Description

The aim of the study is to evaluate the quality of follow-up and treatment by means of consecutive data collection and anonymised analysis of all glaucoma patients of a tertiary university hospital glaucoma service. Parameters being analyzed are: Age, sex, refraction, family history, known duration of glaucoma, highest intraocular pressure before treatment, systemic and topical medication, previous ocular surgery. 24h Goldmann-applanation tonometry, biomicroscopy, gonioscopy, Heidelberg Retinal Tomograph (HRT), glaucoma diagnosis with Scanning-Laser-Polarimetry (GDx), optical coherence tomography (OCT), Pentacam, Ocular Response Analyzer (ORA), Corvis ST (Corneal Visualization with the Scheimpflug Technology), perimetry ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02959242
Study type Observational
Source Technische Universität Dresden
Contact Karin R Pillunat, MD
Phone +49 351 458 3274
Email karin.pillunat@uniklinikum-dresden.de
Status Recruiting
Phase
Start date January 2006
Completion date December 2026

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