OCTA-RVD: Optical Coherence Tomography Angiography in Subjects With Retinal Vascular Disease
Study Details
Study Description
Brief Summary
This study will perform a prospective, longitudinal analysis of clinical and imaging findings from normal controls and subjects with retinal vascular disease to better define the diagnostic imaging criteria that signify change in disease stage. This includes disease progression in early stages of disease or disease regression with appropriate standard-of-care treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The objective of this study is to perform a prospective, longitudinal analysis of clinical and imaging findings from normal controls and subjects with retinal vascular disease to better define the diagnostic imaging criteria that signify change in disease stage. This includes disease progression in early stages of disease or disease regression with appropriate standard-of-care treatment.
Subjects will be identified from healthy subjects (seen for screening eye exams) and diseased subjects undergoing standard-of-care treatment or screening at eye clinic locations. The study population will include subjects with retinal vascular disease including but not limited to diabetic retinopathy, hypertension, retinal vein/arterial occlusion, and macular degeneration. Subjects who are enrolled will undergo non-invasive, minimal risk, FDA approved diagnostic imaging procedures to identify vascular changes.
The study methods will include retrospective review and collection of clinically approved imaging data that is obtained through standard-of-care methods for subjects who meet inclusion and exclusion criteria. Subjects who are identified in this manner will be asked to participate in a prospective study by each clinical study site.
The study end-points include the correlation of diagnostic imaging findings from OCT based images with fundus photographs, clinical disease stage and visual acuity.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Controls Subjects in this group do not have any ocular pathology and are also not hypertensive. Some subjects in this arm will undergo retinal vascular reactivity assessments. |
Device: Swept-Source OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Spectral-Domain OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Fundus Imaging
Non-invasive, minimal risk, ocular imaging study
Device: Axial Length Measurement Device
Non-invasive, minimal risk, ocular imaging study
Other Names:
|
| Other: Diabetics with and without Diabetic Retinopathy Only Subjects in this group only have diabetes with or without diabetic retinopathy. Some subjects in this arm will undergo retinal vascular reactivity assessments. |
Device: Swept-Source OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Spectral-Domain OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Fundus Imaging
Non-invasive, minimal risk, ocular imaging study
Device: Axial Length Measurement Device
Non-invasive, minimal risk, ocular imaging study
Other Names:
|
| Other: Hypertension Only Subjects in this group only have hypertension with or without ocular pathology related to hypertension. Some subjects in this arm may undergo retinal vascular reactivity assessments. |
Device: Swept-Source OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Spectral-Domain OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Fundus Imaging
Non-invasive, minimal risk, ocular imaging study
Device: Axial Length Measurement Device
Non-invasive, minimal risk, ocular imaging study
Other Names:
|
| Other: Diabetics w/ or w/o Diabetic Retinopathy & Hypertension Subjects in this group have diabetes with or without diabetic retinopathy and hypertension with or without ocular pathology related to hypertension. Some subjects in this arm may undergo retinal vascular reactivity assessments. |
Device: Swept-Source OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Spectral-Domain OCT Angiography
Non-invasive, minimal risk, ocular imaging study
Other Names:
Device: Fundus Imaging
Non-invasive, minimal risk, ocular imaging study
Device: Axial Length Measurement Device
Non-invasive, minimal risk, ocular imaging study
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Correlation of Imaging [5 years]
Correlation of diagnostic imaging findings (vessel skeleton density) from OCT based images with disease stage
Eligibility Criteria
Criteria
Exclusion Criteria:
-
Both subjects with diseases and controls:
-
Children (age<18)
-
Pregnant females
-
Developmentally delayed subjects
-
Subjects unable to provide informed consent
-
Inability to cooperate with tests and study instructions
-
Images with motion artifact or signal strength < 7
-
History of glaucoma
-
History of age-related macular degeneration
-
History of any visually significant eye disease
-
History of proliferative diabetic retinopathy
-
History of any inflammatory disease
-
History of heart disease
-
History of thyroid disease.
-
Additional criteria for controls:
-
History of any type of Diabetes Mellitus
-
History of any type of Hypertension
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Wilmer Eye Institute | Baltimore | Maryland | United States | 21287 |
Sponsors and Collaborators
- Johns Hopkins University
- National Eye Institute (NEI)
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- IRB00276904
- R01EY030564