Uveitis/Intraocular Inflammatory Disease Biobank (iBank)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Background: Uveitis is a serious eye disease that can cause vision loss. Treatment sometimes causes serious side effects or does not work. Researchers want to learn more about uveitis and why some people develop it.

Objective: To learn clinical and genetic factors that may make people develop uveitis and influence how they respond to treatment.

Eligibility: People ages 8 and older who have uveitis, scleritis, inflammatory eye disease, or a disease related to eye inflammation INCLUSION CRITERIA FOR COVID-19 COHORT: Participants with COVID-19 will be eligible if they: Have a diagnosis of COVID-19 confirmed by a nasaopharyngeal swab (or another confirmative test) within less than or equal to 3 days prior, with symptoms of any severity. Are able to give verbal consent. Are 16 years of age or older. EXCLUSION CRITERIA FOR COVID-19 COHORT: Participants with COVID-19 will not be eligible if they: Use regular prescription eye drops on the day of sampling. Current use of antiviral medications.

Design: Participants will be screened with: Medical history Physical exam Eye exam Participation lasts up to 10 years. The clinic visit schedule varies depending on participants eye disease: Baseline visit with annual follow-ups Baseline visit, visits at months 3 and 6, and annual follow-ups Another schedule set by the researcher Depending on participants eye disease, tests during each visit could include: Fluorescein angiography or indocyanine green angiography: Dye is injected through a needle in the arm and flows through the blood vessels in the eye. A camera takes pictures of the eye. Electroretinography: Participants sit in the dark with their eyes patched. After 30 minutes, numbing drops and contact lenses are put in the eyes. Then, the retina is stimulated with flashing lights. Perimetry: Participants look into a bowl or lens and press a button when they see a light. Conjunctival or corneal biopsy, or skin biopsy: A small piece of tissue is removed. Anterior chamber tap: A needle enters the eye to remove fluid. Blood and urine tests Saliva, stool, hair, or tear samples Cotton swab of the inside of the cheek. During the study, participants may need immunosuppressive treatment, such as drugs or injections in or around the eyes depending on their disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 8
Healthy Volunteers: Accepts Healthy Volunteers
View:

• Participants will be eligible if they:

• Have a diagnosis of uveitis, scleritis or a disease known to be associated with intraocular inflammation, (e.g., sarcoidosis, Behcet's disease, MS and lymphoma) OR could serve as an unaffected control.

• Are eight years of age or older if an affected participant.

• Are 18 years of age or older if serving as an unaffected control.

• For participants 18 years of age and older:

• Are willing to give informed consent that includes collection and study of at least one peripheral blood sample.

• Participants with COVID-19 will be eligible if they:

• Have a diagnosis of COVID-19 confirmed by a nasopharyngeal swab (or another confirmative test) within less than or equal to 3 days prior, with symptoms of any severity.

• Are able to give verbal consent.

• Are 16 years of age or older.

Locations
United States
Maryland
National Institutes of Health Clinical Center
Recruiting
Bethesda
Contact Information
Primary
Patti Sherry, C.R.N.O.
patti.sherry@nih.gov
(301) 435-4529
Backup
Shilpa M Kodati, M.D.
shilpa.kodati@nih.gov
(301) 496-5847
Time Frame
Start Date: July 26, 2016
Estimated Completion Date: December 31, 2029
Participants
Target number of participants: 650
Treatments
Anterior Uveitis
Participants with AU at entry
Intermediate Uveitis
Participants with IU at entry
Other
Participants not fitting above criteria
Posterior/Pan Uveitis
Participants with non-infectious posterior or pan-uveitis
Related Therapeutic Areas
Sponsors
Leads: National Eye Institute (NEI)

This content was sourced from clinicaltrials.gov

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