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NCT02959242 Clinical Trial

Dresden Glaucoma and Treatment Study (DGTS)

Glaucoma Clinical Trial

Official title:
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.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02959242
Other study ID # DGTS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2006
Est. completion date December 2026

Study information
Verified date September 2023
Source Technische Universität Dresden
Contact Karin R Pillunat, MD
Phone +49 351 458 3274
Email karin.pillunat@uniklinikum-dresden.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

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

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - manifest glaucoma, ocular Hypertension, glaucoma suspect Exclusion Criteria: - under 18 years of age, corneal diseases

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Germany University Eye Hospital, Medical Faculty, Technical University Dresden Dresden Saxony

Sponsors (1)
Lead Sponsor Collaborator
Technische Universität Dresden

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Follow-up intervals To find the best follow-up intervals for glaucoma patients. 20 years
Secondary Assessment of treatment quality What is the best treatment option for the individual patient? 20 years
Secondary 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 Diurnal intraocular pressure, best corrected visual acuity, visual fields 20 years
Secondary 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 surgery Diurnal intraocular pressure, best corrected visual acuity, visual fields 20 years
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