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Clinical Trials/NCT02959242
NCT02959242
Recruiting
Not Applicable

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.

Technische Universität Dresden1 site in 1 country10,000 target enrollmentJanuary 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glaucoma
Sponsor
Technische Universität Dresden
Enrollment
10000
Locations
1
Primary Endpoint
Follow-up intervals
Status
Recruiting
Last Updated
last year

Overview

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

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
December 2030
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Karin Pillunat

Dr. med.

Technische Universität Dresden

Eligibility Criteria

Inclusion Criteria

  • manifest glaucoma, ocular Hypertension, glaucoma suspect

Exclusion Criteria

  • under 18 years of age, corneal diseases

Outcomes

Primary Outcomes

Follow-up intervals

Time Frame: 20 years

To find the best follow-up intervals for glaucoma patients.

Secondary Outcomes

  • Assessment of treatment quality(20 years)
  • 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(20 years)
  • 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(20 years)

Study Sites (1)

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