Skip to content

Dresden Glaucoma and Treatment Study (DGTS)

Dresden Glaucoma and Treatment Study: Analysis to Assure the Quality of Follow-up and Therapy of Glaucoma Patients in a Tertiary University Hospital Glaucoma Service.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02959242
Enrollment
10000
Registered
2016-11-09
Start date
2006-01-01
Completion date
2032-12-01
Last updated
2026-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, Glaucoma, Angle-Closure, Glaucoma, Low Tension, Glaucoma, Open-Angle

Keywords

Follow-up intervals, Treatment Efficiency, Laser Therapy, Glaucoma Surgery, Minimal Invasive Glaucoma Surgery (MIGS)

Brief summary

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

Detailed 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

Interventions

None listed

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* manifest glaucoma, ocular Hypertension, glaucoma suspect

Exclusion criteria

* under 18 years of age, corneal diseases

Design outcomes

Primary

MeasureTime frameDescription
Follow-up intervals20 yearsTo find the best follow-up intervals for glaucoma patients.

Secondary

MeasureTime frameDescription
Assessment of treatment quality20 yearsWhat is the best treatment option for the individual patient?
Assessment of intraocular pressure-lowering efficacy and number of participants with treatment-related adverse events as assessed by CTCAE v4.0 of glaucoma laser therapy20 yearsDiurnal intraocular pressure, best corrected visual acuity, visual fields
Assessment of intraocular pressure-lowering efficacy and number of participants with treatment-related adverse events as assessed by CTCAE v4.0 of glaucoma laser therapy of glaucoma surgery20 yearsDiurnal intraocular pressure, best corrected visual acuity, visual fields

Countries

Germany

Contacts

CONTACTKarin R Pillunat, MD
karin.pillunat@uniklinikum-dresden.de+49 351 458 3274
CONTACTLutz E Pillunat, MD, PhD
lutze.pillunat@uniklinikum-dresden.de+49 351 458 3381
STUDY_DIRECTORLutz E Pillunat, MD, PhD

Medical faculty of the Technical University of Dresden, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026