SBIR/STTR Research Award

Noninvasive Device for Sealing Vascular Access Punctures

Award identifier 7128c5fe540ddcf3d4f1ade4cb3d950f4742145f2a82351b2669215bf4481c8aAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$899,660

Program and phase

SBIR · Phase II

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
THERUS CORPORATION
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Despite dramatic advances in the battle against cardiovascular disease, sealing of the femoral arteriotomy following percutaneous, transcatheter procedures remains a major challenge In the United States alone, over 48 million of these procedures are performed annually Manual compression is the most widely used method for achieving arteriotomy hemostasis However, compression is very time consuming and requires significant hospital resources Moreover, patients report that the most painful aspects of their catheterization experience are the manual compression of their catheterization site and having to lie immobile for hours so as not to disrupt healing of their arteriotomy A number of commercial devices to seal catheter wounds have been developed and are being marketed, however, these devices have drawbacks--they are invasive, expensive, difficult to use and leave behind foreign material In our Phase I effort, we demonstrated that high intensity focused ultrasound (HIFU) can successfully be used to noninvasively seal arteriotomies in large laboratory animals and, subsequently, in humans subjects In this Phase II application, we propose to (1) develop a clinical-level prototype device that uses ultrasound imaging and HIFU to facilitate noninvasive femoral arteriotomy sealing, (2) conduct key preclinical studies in an animal model, and (3) design and develop a phase I clinical trial protocol In Phase III, human clinical trials would be performed and product commercialization would commence.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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