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Quality of Life and Visual Function in Uveitis Patients

T

The New York Eye & Ear Infirmary

Status

Unknown

Conditions

Uveitis
Anterior Uveitis
Posterior Uveitis
Panuveitis

Study type

Observational

Funder types

Other

Identifiers

NCT00407316
07-A-6803

Details and patient eligibility

About

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.

Full 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.

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial contacts and locations

1

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Central trial contact

Katy W Tai, MA

Data sourced from clinicaltrials.gov

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