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Quality of Life and Visual Function in Uveitis Patients

NCT ID: NCT00407316

Last Updated: 2006-12-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-06-30

Study Completion Date

2006-11-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Anterior Uveitis Posterior Uveitis Panuveitis Uveitis

Keywords

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Uveitis Quality of life Visual function

Study Design

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Observational Model Type

DEFINED_POPULATION

Study Time Perspective

OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The New York Eye & Ear Infirmary

OTHER

Sponsor Role lead

Principal Investigators

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C. Michael Samson, MD

Role: PRINCIPAL_INVESTIGATOR

New York Eye and Ear Infirmary

Locations

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New York Eye and Ear Infirmary

New York, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Katy W Tai, MA

Role: CONTACT

Phone: 212-979-4251

Email: [email protected]

Facility Contacts

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Katy W Tai, MA

Role: primary

Other Identifiers

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07-A-6803

Identifier Type: -

Identifier Source: org_study_id