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NCT00407316 Clinical Trial

Quality of Life and Visual Function in Uveitis Patients

Uveitis Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00407316
Other study ID # 07-A-6803
Secondary ID
Status Recruiting
Phase Phase 0
First received December 2, 2006
Last updated December 4, 2006
Start date June 2006
Est. completion date November 2006

Study information
Verified date December 2006
Source The New York Eye & Ear Infirmary
Contact Katy W Tai, MA
Phone 212-979-4251
Email ktai@nyee.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date November 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 95 Years
Eligibility 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

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
United States New York Eye and Ear Infirmary New York New York

Sponsors (1)
Lead Sponsor Collaborator
The New York Eye & Ear Infirmary

Country where clinical trial is conducted

United States, 

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