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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02357238
Other study ID # 11-087
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2011
Est. completion date January 2030

Study information

Verified date February 2024
Source The Cleveland Clinic
Contact Kimberly M Baynes, BSN, RN, COA
Phone 216-444-2566
Email baynesk@ccf.org
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

In order to improve the investigators knowledge about uveitis and the underlying mechanism of disease, the investigators propose collecting blood from patients with uveitis, isolating DNA and sequencing the DNA to identify genetic mutations or associations in these patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date January 2030
Est. primary completion date January 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria: - Any patient above with the diagnosis of uveitis. - Any patient with a diagnosis of infectious uveitis such as toxoplasmosis retinochoroiditis, herpes associated retinitis. Exclusion Criteria: - Patients who are unable to give consent - Patients in whom an adequated blood sample can not be obtained.

Study Design


Locations

Country Name City State
United States Cleveland Clinic Foundation Cleveland Ohio

Sponsors (1)

Lead Sponsor Collaborator
The Cleveland Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Non infectious uveitis Distinct uveitis conditions will have a polymorphism association or specific mutation. 5 years
Secondary Infectious uveitis Infectious uveitis (such as herpes associated uveitis, toxoplasmosis retinochoroiditis) will have specific polymorphisms/mutations in innate immune system genes which predispose the patient to infectious uveitis. 5 years
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