Dry Macular Degeneration Clinical Trial
— BIRC-01Official title:
Non Exudative Age-Related Macular Degeneration Imaged With Swept Source Optical Coherence Tomography
Verified date | March 2022 |
Source | Boston Image Reading Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The investigators wish to better understand the role of the choriocapillaris (CC) in the formation and progression of non-exudative in age related macular degeneration (armd) by imaging the retinal pigment epithelium (rpe) and the choroidal microvasculature and by studying their inter-dependence to determine if the loss of the CC could prove useful as an anatomic clinical trial endpoint in future drug trials.
Status | Active, not recruiting |
Enrollment | 225 |
Est. completion date | March 2023 |
Est. primary completion date | March 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years and older |
Eligibility | Inclusion Criteria: 1. Aged 50 and over 2. Clinic diagnosis of non-exudative iAMD in at least one eye with a drusen volume in the central 3 mm circle centered on the fovea of at least 0.02 mm3 in the absence of GA or nGA as diagnosed with OCT en face imaging OR Clinical diagnosis of early or early/intermediate stage AMD in one eye in the absence of nGA or GA and exudative AMD in the other eye OR clinical diagnosis of GA or nGA secondary to AMD that is at least the size of a large druse (125 microns in diameter; 0.05 mm2) and no greater than 7 disc areas (17 mm2) in at least one eye which has never been treated with anti-VEGF agents 3. Willing and able to comply with clinic visits and study-related procedures 4. Provide signed informed consent Exclusion Criteria: A subject who meets any of the following criteria will be excluded from the study: 1. Below the age of 50 2. Subjects with exudative AMD in both eyes 3. Eyes with evidence of non-proliferative and proliferative diabetic retinopathy. 4. Presence of confounding ocular diagnosis such as myopia >6D, or other ocular conditions that may cause retinal pigment epithelium atrophy or exudative MNV 5. Subjects unable to give informed consent. 6. Subjects who are unable to comply with imaging guidelines |
Country | Name | City | State |
---|---|---|---|
Australia | Melbourne University CERA | East Melbourne | Victoria |
United States | New England Eye Center/Tufts Medical Center | Boston | Massachusetts |
United States | University of California Los Angeles Doheny Eye Institute | Los Angeles | California |
United States | Bascom Palmer Eye Institue | Miami | Florida |
United States | Vitreous Retina Macular Consultants of NY | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Boston Image Reading Center |
United States, Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Choroidal Perfusion Deficits at 1 year compared to Baseline | Assessment of Choriocapillaris perfusion | 1 year time point | |
Secondary | Pre-existing sub-clinical Macular Neovascularization (MNV) | Presence of abnormal new vessels arising from the Choroid | 1 year and 2-year time points | |
Secondary | Automated Drusen Volume measurements | Compare the automated measurements of drusen volume using the Zeiss algorithm with manual measurements by trained readers | 1 year and 2-year time points | |
Secondary | Automated GA measurements | Compare the automated measurements of GA area using the Zeiss algorithm with manual measurements by trained readers | 1 year and 2-year time points | |
Secondary | Structural OCT markers and Genetic Markers | Correlate structural markers on SS-OCT/OCTA with genetic markers of disease | 1 year and 2-year time points |
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