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Acute Anterior Uveitis: Psychic Burden and Pain

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified November 2011 by Saskia M Maca, Hospital Hietzing.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01156285
First Posted: July 2, 2010
Last Update Posted: November 29, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Medical University of Graz
Information provided by (Responsible Party):
Saskia M Maca, Hospital Hietzing
  Purpose

Acute anterior uveitis (AU) is a common reason for attendance at ophthalmic outpatient clinics. The painfulness and the fear of a transient or even persistent loss of vision may markedly reduce the individual's subjective well-being and pose a psychological burden.

This study will test the hypothesis that during an attack of AU the patient experiences a marked reduction in psychological and physical well-being.

Prospective, hospital-based epidemiologic study using a patient questionnaire with standardized psychological tests and a pain scale.


Condition Intervention
Anterior Uveitis Other: Filling in a patient questionnaire

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Acute Anterior Uveitis: Psychic Burden and Pain

Resource links provided by NLM:


Further study details as provided by Saskia M Maca, Hospital Hietzing:

Estimated Enrollment: 35
Study Start Date: May 2010
Estimated Study Completion Date: June 2012
Groups/Cohorts Assigned Interventions
AAU
patient with acute attack of anterior uveitis
Other: Filling in a patient questionnaire
Filling in a patient questionnaire

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with acute attack of anterior uveitis
Criteria

Inclusion Criteria:

  • Acute attack of anterior uveitis

Exclusion Criteria:

  • Other forms of uveitis
  • Chronic anterior uveitis
  • Therapy started
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01156285


Contacts
Contact: Saskia M Maca, MD +43-1-80110 ext 2266 Saskia.Maca@wienkav.at

Locations
Austria
Department of Ophthalmology, Medical University Graz Not yet recruiting
Graz, Styria, Austria
Contact: Andreas Wedrich, MD, Prof.    43-316-385 ext 2394      
Principal Investigator: Andreas Wedrich, MD, Prof         
Sub-Investigator: Julia Wagner, MD         
Department of Ophthalmology, Hietzing Hospital Recruiting
Vienna, Austria, 1130
Principal Investigator: Saskia M Maca, MD         
Sponsors and Collaborators
Hospital Hietzing
Medical University of Graz
Investigators
Study Director: Saskia M Maca, MD Hospital Hietzing
  More Information

Responsible Party: Saskia M Maca, MD, Hospital Hietzing
ClinicalTrials.gov Identifier: NCT01156285     History of Changes
Other Study ID Numbers: MAC110
First Submitted: July 1, 2010
First Posted: July 2, 2010
Last Update Posted: November 29, 2011
Last Verified: November 2011

Additional relevant MeSH terms:
Uveitis
Uveitis, Anterior
Iridocyclitis
Uveal Diseases
Eye Diseases
Panuveitis
Iris Diseases