Quality of Life in Patients With Intermediate Uveitis

This study has been completed.
Information provided by:
St. Franziskus Hospital
ClinicalTrials.gov Identifier:
First received: March 11, 2011
Last updated: July 19, 2011
Last verified: March 2011
The aim of this study is to determine if macular edema is associated with less visual function and quality of live in patients with intermediate uveitis

Macular Edema

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Influence of Macular Edema on Quality of Life in Patients With Non-infectious Intermediate Uveitis

Resource links provided by NLM:

Further study details as provided by St. Franziskus Hospital:

Patients with intermediate uveitis


Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with intermediate uveitis

Inclusion Criteria:

  • Pars planitis

Exclusion Criteria:

  • Patients with any other diseases
  • Patients under age 18
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01314469

Department of Ophthalmology at St Franziskus Hospital
Muenster, Germany, 48145
Sponsors and Collaborators
St. Franziskus Hospital
  More Information

ClinicalTrials.gov Identifier: NCT01314469     History of Changes
Other Study ID Numbers: 2008-559-f-S 
Study First Received: March 11, 2011
Last Updated: July 19, 2011
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by St. Franziskus Hospital:
Quality of life in patients with macular edema compared to patients without macular edema.

Additional relevant MeSH terms:
Macular Edema
Pars Planitis
Uveitis, Intermediate
Choroid Diseases
Eye Diseases
Macular Degeneration
Retinal Degeneration
Retinal Diseases
Uveal Diseases
Uveitis, Posterior

ClinicalTrials.gov processed this record on May 24, 2016