Quality of Life and Visual Function in Uveitis Patients

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2006 by The New York Eye & Ear Infirmary.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
The New York Eye & Ear Infirmary
ClinicalTrials.gov Identifier:
NCT00407316
First received: December 2, 2006
Last updated: December 4, 2006
Last verified: December 2006
  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
Phase 0

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

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

Ages Eligible for Study:   18 Years to 95 Years
Genders Eligible for Study:   Both
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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

ClinicalTrials.gov Identifier: NCT00407316     History of Changes
Other Study ID Numbers: 07-A-6803
Study First Received: December 2, 2006
Last Updated: December 4, 2006
Health Authority: United States: Institutional Review Board

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

Additional relevant MeSH terms:
Uveitis
Chorioretinitis
Panuveitis
Uveitis, Anterior
Iridocyclitis
Uveitis, Posterior
Uveal Diseases
Eye Diseases
Retinitis
Retinal Diseases
Choroiditis
Choroid Diseases
Iris Diseases

ClinicalTrials.gov processed this record on September 22, 2014