SBIR/STTR Research Award

A Bullet Proof vascular graft to prevent dialysis access cannulation injury

Award identifier 984f7ad066be8de8788fc8dcd02296e08069af3583d3b10777fdfcb093077316Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$150,000

Program and phase

STTR · Phase I

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Innavasc Medical, Inc.
Proposal award date
2016-09-01
Contract end date
2017-08-31
UEI
GSH6GDCYLQN5
Solicitation number
PA15-270
Topic code
400

Research abstract

Project Summary Abstract Synthetic arteriovenous grafts AVGs can provide life sustaining vascular access for dialysis patients but are subject to multiple modes of failure and complications related to chronic needle cannulation poor graft identification delayed access and bleeding These graft needle cannulation associated complications translate to millions of dollars in health care expenses hospitalizations pain and suffering To address this problem we have developed an immediate access hemodialysis graft that assures routine error free successful cannulation and prevents graft injury the Bullet Proof vascular graft This novel graft has been designed to be hemostatic durable easily identifiable and usable by dialysis technicians and patients alike In preliminary testing the Bullet Proof graft has been shown to be hemostatic self sealing resistant to posterior and sidewall penetration and more durable than current standard and early access dialysis grafts available for clinical use In this Phase I STTR application we will improve upon the current design of the Bullet Proof vascular graft Aim and will conduct a series of rigorous experiments to validate our pilot studies These experiments will consist of bench top testing designed to evaluate the self sealing resistance to back wall penetration and overall graft durability of our graft design when compared to that of the leading standard and early access vascular access grafts on the market today Aim The safety and effectiveness of our graft design will also be tested in vivo using a porcine dialysis graft cannulation model Aim In these experiments test and control grafts will be implanted and cannulated for up to weeks and evaluated for overall graft patency time to hemostasis and resistance to posterior graft wall injury Successful completion of this Phase I STTR project will result in an improved version of the Bullet Proof AVG approaching a finalized manufacturable design validation of the key design attributes of the graft and verification of the safety efficacy and patency of this novel dialysis graft technology Project Narrative Arteriovenous grafts AVGs are required by those with kidney failure in order to clear the toxins and excess fluid from their blood hemodialysis and injuries and complications of these AVGs are extremely common and result in infection pain and suffering These complications lead to millions in health care expenditures and the graftandapos s immediate use feature could eliminate the need for dialysis catheters which lead to expensive and deadly blood stream infections Our team has developed an immediate access hemodialysis graft that has been designed to be easily identifiable and usable by dialysis technicians and patients alike and assures routine error proof successful cannulation and prevents graft injury

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

5 SBIR/STTR records share this UEI (2016–2020). Reported award amounts total $6,122,433. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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