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Non Exudative AMD Imaged With SS-OCT

Non Exudative Age-Related Macular Degeneration Imaged With Swept Source Optical Coherence Tomography

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03688243
Acronym
BIRC-01
Enrollment
225
Registered
2018-09-28
Start date
2018-01-18
Completion date
2023-03-31
Last updated
2022-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry Macular Degeneration

Keywords

AMD, early AMD, intermediate AMD, Geographic Atrophy, nascent GA

Brief summary

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.

Detailed description

This is a longitudinal observational study where the investigators will look at 450 subjects, 200 with intermediate AMD in at least one eye, or with AMD in one eye, either early or intermediate, and with late AMD (exudative) in the other eye, and 250 subjects with nGA or GA in at least one eye.

Interventions

All subjects will undergo retinal imaging using the Zeiss PlexElite SS-OCT, a non-contact, non-invasive ocular imaging instrument

Sponsors

Boston Image Reading Center
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in Choroidal Perfusion Deficits at 1 year compared to Baseline1 year time pointAssessment of Choriocapillaris perfusion

Secondary

MeasureTime frameDescription
Pre-existing sub-clinical Macular Neovascularization (MNV)1 year and 2-year time pointsPresence of abnormal new vessels arising from the Choroid
Automated Drusen Volume measurements1 year and 2-year time pointsCompare the automated measurements of drusen volume using the Zeiss algorithm with manual measurements by trained readers
Automated GA measurements1 year and 2-year time pointsCompare the automated measurements of GA area using the Zeiss algorithm with manual measurements by trained readers
Structural OCT markers and Genetic Markers1 year and 2-year time pointsCorrelate structural markers on SS-OCT/OCTA with genetic markers of disease

Countries

Australia, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026