SBIR-STTR Award

Ultrahigh Speed OCT Angiography System for Patients who are Unable to Cooperate
Award last edited on: 2/14/2024

Sponsored Program
SBIR
Awarding Agency
NIH : NEI
Total Award Amount
$456,163
Award Phase
1
Solicitation Topic Code
867
Principal Investigator
Christian Viehland

Company Information

Theia Imaging LLC

201 West Main Street
Durham, NC 27701
   (919) 323-0067
   N/A
   www.theiaimaging.com
Location: Single
Congr. District: 04
County: Orange

Phase I

Contract Number: 1R43EY034418-01
Start Date: 9/1/2022    Completed: 8/31/2023
Phase I year
2022
Phase I Amount
$259,603
Systemic and ocular diseases affecting retinal vascular development, perfusion, and neovascularization are preventable causes of moderate to severe vision impairment in millions of people worldwide. While many adults can cooperate with and hold still for advanced retinal imaging, a significant number of patients including infants, young children, and older patients who, due to sickness, mobility, anesthesia, or a variety of other reasons, are unable to cooperate (I/Y/UC patients) cannot. These patients are often the youngest and/or sickest patients who are at the highest risk of vascular, neurovascular, or ischemic disease that can affect the eye. At present, these patients cannot access advanced imaging technologies that would provide valuable diagnostic information and would contribute to advancing our understanding of their diseases. Optical coherence tomography (OCT) is the gold standard for diagnosis of retinal diseases. OCT angiography (OCTA) is a functional extension of OCT that enables non-invasive, depth resolved imaging of retinal microvasculature without the need for exogenous contrast agents. Because of its dense sampling requirements, OCTA requires long scans and compliant patients who can hold their head and eyes steady. While large tabletop systems can simplify imaging with active tracking, I/Y/UC patients typically cannot position at a chinrest for the duration of the scan. We believe that the development of an ultra-high-speed commercial handheld OCTA device would provide physicians a valuable research and diagnostic tool for imaging of these underserved patients. Under previous NIH funding, Theia Imaging has developed the T1 system, a portable OCT device with a light-weight HH-OCT probe. Here, we propose to develop the T1-A, an ultra-high-speed upgrade to the T1 system that can bring state-of-the-art OCTA imaging to bedside. This will be achieved through the following Specific Aims. Aim 1: Development of an ultra-high-speed handheld OCTA system. We will develop an ultra- high-speed OCT device by upgrading components in the existing T1 OCT. Aim 2: Development of OCTA acquisition and processing software. We will develop OCTA capture and visualization software, including a novel high-speed aiming mode and capable of providing real-time feedback, even at these extremely high scan rates. Aim 3: Validation study. We will demonstrate system feasibility by conducting a validation study evaluating the performance of the T1-A system. The expected outcome of this proposal is the development of an ultra-high-speed, handheld OCTA imaging tool, ready for clinician-scientists and caregivers to use to gather vascular data that would otherwise be inaccessible. This tool will improve the care of these underserved populations. Upon successful completion of this project, we will submit a follow-on Phase II proposal to the system, construct additional prototype devices, and work with collaborators to perform a multi-center clinical study to obtain necessary validation data for 510(k) and other regulatory clearances.

Public Health Relevance Statement:
NARRATIVE Systemic and ocular diseases affecting retinal vascular development, perfusion, and neovascularization are preventable causes of moderate to severe vision impairment in millions of people worldwide. While many adults can cooperate with and hold still for advanced retinal imaging, a significant number of patients (including infants, young children, and older patients who are unable to cooperate) cannot, and thus cannot access these advanced imaging technologies that provide valuable diagnostic information and advance our understanding of disease. In this Small Business Innovation Research proposal, we propose to develop an ultra-high-speed handheld OCTA device that will provide physicians a valuable research and diagnostic tool for imaging of these underserved patients.

Project Terms:
Adult; 21+ years old; Adult Human; adulthood; Affect; Anesthesia procedures; Anesthesia; Angiography; Angiogram; angiographic imaging; Blood Vessels; vascular; Child; 0-11 years old; Child Youth; Children (0-21); youngster; Clinical Research; Clinical Study; Contrast Media; Contrast Agent; Contrast Drugs; Radiopaque Media; Diagnosis; Disease; Disorder; Dyes; Coloring Agents; Eye; Eyeball; Feedback; Fluorescein Angiography; Gold; Head; Human; Modern Man; Infant; intravenous injection; Longevity; Length of Life; life span; lifespan; Motion; Persons; NIH; National Institutes of Health; United States National Institutes of Health; nystagmus; Pathologic Nystagmus; Patients; Perfusion; Physicians; Research; Investigators; Researchers; Research Personnel; Research Proposals; Retina; Retinal Disorder; retina disease; retina disorder; retinopathy; Retinal Diseases; Retrolental Fibroplasia; premature retinopathy; Retinopathy of Prematurity; Risk; Software; Computer software; Time; Translations; Vascular Diseases; Vascular Disorder; blood vessel disorder; vascular dysfunction; vasculopathy; Visual impairment; Diminished Vision; Low Vision; Partial Sight; Reduced Vision; Subnormal Vision; vision impairment; visually impaired; Work; Fluorescein; Caregivers; Care Givers; Intensive Care; Developmental Delay Disorders; Developmental Delay; Specific Child Development Disorders; Caring; improved; Fundus photography; eye fundus photography; fundus camera; Phase; insight; awake; Funding; Dysfunction; Physiopathology; pathophysiology; Functional disorder; lightweight; light weight; tool; Scientist; Scanning; Protocol; Protocols documentation; System; interest; Performance; success; Speed; Structure; novel; validation studies; Devices; Position; Positioning Attribute; Fundus; Sampling; portability; Optical Coherence Tomography; Doppler OCT; OCT Tomography; optical Doppler tomography; optical coherence Doppler tomography; diagnosis standard; Data; Imaging Instrument; Imaging Tool; Imaging Device; Small Business Innovation Research Grant; SBIR; Small Business Innovation Research; Update; Validation; sample fixation; Fixation; Development; developmental; Image; imaging; neovascularization; imaging probe; Underserved Population; under served group; under served people; under served population; underserved group; underserved people; design; designing; neonatal hypoxic-ischemic brain injury; hypoxic ischemic encephalopathy; neonatal HIE; neonatal hypoxia-ischemia; neonatal hypoxic-ischemic encephalopathy; macula; macular; older patient; elderly patient; Visualization software; visualization tool; Outcome; three dimensional structure; 3-D structure; 3-dimensional structure; 3D structure; Imaging technology; two-dimensional; 2-dimensional; prototype; high risk; patient population; treatment response; response to therapy; response to treatment; therapeutic response; therapy response; Institutional Review Boards; IRB; IRBs; pediatric patients; child patients; neurovascular; neuro-vascular; imager; retinal imaging; retina imaging; Multi-site clinical study; Multi-center clinical study; Multicenter clinical study; Multisite clinical study; diagnostic tool; diagnostic value; diagnostic ability; diagnostic capability; diagnostic power; diagnostic utility

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
$196,560