Optical Coherence Tomography (OCT) in Retinal Vasculitis

Retinal Vasculitis Clinical Trial

Official title:

Evaluation of the Utility of OCT Angiography in Assessing Vascular Perfusion in Retinal Vasculitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01998464
• Other study ID #: OHSU IRB#00010137
• Status: Completed
• Start date: January 2014
• Est. completion date: August 23, 2018

Study information

• Verified date: February 2024
• Source: Oregon Health and Science University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Retinal vasculitis is a sight-threatening inflammation that involves the blood vessels of the retina, the tissue that lines the inside of the eye. This inflammation may occur on its own or as a result of an infectious, cancerous, or inflammatory disorder.

Optical coherence tomography (OCT) is an imaging technology that can perform non-contact cross-sectional imaging of retinal and choroidal tissue structure in real time. It is similar to ultrasound imaging, except that OCT measures the intensity of reflected light rather than sound waves.

The purpose of this study is to see if non-invasive OCT technology can diagnose retinal vasculitis as well as the more invasive fluorescein angiography, which requires an injection of dye into the vein of an arm of a patient. The study will also compare the mapping of blood vessels (angiography) and loss of blood flow (ischemia) by fluorescein angiography and OCT.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: August 23, 2018
• Est. primary completion date: August 23, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of retinal vasculitis

Exclusion Criteria:

• Inability to give informed consent.

• Inability to complete the qualifying study tests within a 30 day period from date of enrollment

• Significant renal disease, defined as a history of chronic renal failure requiring dialysis or kidney transplant.

• A prior history of reaction to fluorescein or other dyes.

• A condition that, in the opinion of the investigator, would preclude participation in the study (e.g. unstable medical status including blood pressure, cardiovascular disease, and glycemic control).

• Blood pressure > 180/110 (systolic above 180 OR diastolic above 110). If blood pressure is brought below 180/110 by anti-hypertensive treatment, subject can become eligible.

• Systemic anti-vascular endothelial growth factor (VEGF) or pro-VEGF treatment within 4 months prior to treatment.

• Women of child-bearing potential: pregnant or lactating or intending to become pregnant within the next 12 months due to unknown safety of fluorescein angiography.

• Prior panretinal photocoagulation (PRP) or focal laser that would alter the macular perfusion and retinovascular features.

• Inability to maintain stable fixation for OCT imaging.

• Other ocular condition is present such that, in the opinion of the investigator, may alter the retinal perfusion.

• An ocular condition is present that, in the opinion of the investigator, might affect or alter visual acuity during the course of the study (i.e. cataract)

• Substantial cataract that, in the opinion of the investigator, is likely to decrease visual acuity by 3 lines or more (i.e. cataract would be reducing acuity to 20/40 or worse if the eye was otherwise normal).

• Media opacity or otherwise that would prevent either fixation or ability to obtain adequate images as determined by the examiner.

• History of major ocular surgery (including vitrectomy, cataract extraction, scleral buckle, any intraocular surgery, etc) within prior 4 months.

Related Conditions & MeSH terms

• Retinal Vasculitis
• Vasculitis

Locations

Country	Name	City	State
United States	OHSU	Portland	Oregon

Sponsors (1)

Lead Sponsor	Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Blood flow patterns in retinal vasculitis	To determine if identifying early changes in blood vessel patterns will aid in early diagnosis and treatment of retinal vasculitis. Total retinal blood flow will be measured in uL/min.	24 months
Secondary	Ischemia in retinal vasculitis	To determine if identifying lost or reduced blood flow will aid in early diagnosis and treatment of retinal vasculitis. Non-perfusion area will be measured in mm2.	24 months