SBIR/STTR Research Award

Self-sealing needle guide system for reliable hemodialysis

Award identifier facb0a1386d83e9a617a68d06386b823085aba9c8d2a1da83056cb4d31b87239Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$379,836

Program and phase

SBIR · Phase I

Award year

2024

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Flowpoint Medical Inc
Proposal award date
2024-09-17
Contract end date
2025-11-30
UEI
EJFFEGNXQ2P8
Solicitation number
PA25-212
Topic code
400

Research abstract

PROJECT SUMMARY More than 500,000 Americans are living with end-stage kidney disease, and most of them require life- sustaining hemodialysis treatments three times a week. Despite major improvements over the past several decades, the average life expectancy for dialysis patients is still only 5-10 years. Moreover, the financial burden is significant: dialysis patients comprise about 1% of those on Medicare, yet their care accounts for over 7% of the Medicare budget. There is a pressing need to improve both patient outcomes and the cost-effectiveness of hemodialysis treatment; the single most important problem facing patients being treated with hemodialysis is safe and reliable cannulation. To address these challenges, we developed an implantable device that aims to improve vascular access. The device features a 3D-printed titanium shell that accurately guides the hemodialysis needle to the correct insertion point, while a titanium-nitride coated valve stops bleeding immediately upon needle removal. This new cutting-edge device minimizes the risks for infection, incorrect needle placement, and excessive bleeding, making hemodialysis treatments safer, more efficient, and easier to administer. In this phase- I SBIR proposal, we will use state-of-the-art materials and engineering techniques to refine the manufacturability and operational parameters of our device. Then through a large animal preclinical study, we will evaluate device functionality, tissue integration, inflammatory profile as well as infection and bleeding risks. Our results will pave the way for a comprehensive large-scale GLP-certified animal study and a first-in-human trial. Our device has the potential to be a disruptive technology in nephrology, improve the quality of life for dialysis patients, and possibly facilitate wider adoption of home-based hemodialysis treatments.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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