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Quality of Life and Visual Function in Uveitis Patients

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 December 2006 by The New York Eye & Ear Infirmary.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00407316
First Posted: December 5, 2006
Last Update Posted: December 5, 2006
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.
Information provided by:
The New York Eye & Ear Infirmary
  Purpose
The purpose of this study was to measure the quality of visual function and quality of daily living in patients with anterior, posterior, and panuveitis.

Condition Phase
Anterior Uveitis Posterior Uveitis Panuveitis Uveitis Early Phase 1

Study Type: Observational
Study Design: Observational Model: Defined Population
Primary Purpose: Screening
Time Perspective: Cross-Sectional
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by The New York Eye & Ear Infirmary:

Estimated Enrollment: 50
Study Start Date: June 2006
Estimated Study Completion Date: November 2006
Detailed Description:
The National Eye Institute Visual Functioning Questionnaire, version August 2000 (NEI VFQ-25) and the Medical Outcomes Study (MOS) 36 Item Short Form Health Survey Instrument (SF-36) (RAND 36-Item Health Survey 1.0 Questionnaire) will be administered by a trained interviewer. Socio-demographic and clinical data will be collected for additional QOL parameter.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 95 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Ability to provide written informed consent
  • Subjects of either gender
  • Age greater than or equal to 18 years of age
  • Diagnosed with Uveitis
  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): NCT00407316


Contacts
Contact: Katy W Tai, MA 212-979-4251 ktai@nyee.edu

Locations
United States, New York
New York Eye and Ear Infirmary Recruiting
New York, New York, United States, 10003
Contact: Katy W Tai, MA    212-979-4251    ktai@nyee.edu   
Principal Investigator: C. Michael Samson, MD         
Sponsors and Collaborators
The New York Eye & Ear Infirmary
Investigators
Principal Investigator: C. Michael Samson, MD New York Eye and Ear Infirmary
  More Information

ClinicalTrials.gov Identifier: NCT00407316     History of Changes
Other Study ID Numbers: 07-A-6803
First Submitted: December 2, 2006
First Posted: December 5, 2006
Last Update Posted: December 5, 2006
Last Verified: December 2006

Keywords provided by The New York Eye & Ear Infirmary:
Uveitis
Quality of life
Visual function

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