SBIR/STTR Research Award

Chitosan Endoluminal Hemostatic Dressing

Award identifier 2c05601578912fb05c07bd8b3ce3bced68f2a0034b28389a8e905abce38363d4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$892,569

Program and phase

STTR · Phase II

Award year

2014

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
HemCon Medical Technologies Inc
Proposal award date
2014-09-20
Contract end date
2016-08-31
UEI
Not reported
Solicitation number
PA13-235
Topic code
400

Research abstract

DESCRIPTION provided by applicant Perioperative hemorrhage remains the major complication of transurethral and open prostatic surgical procedures Significant blood loss from these procedures causes delayed healing and longer hospitalization which significantly increases the cost of patient care Moreover prolonged urethral catheterization due to significant post operative hematuria is one of the major causes of discomfort and increases the morbidity to the patients after prostatic surgery Our goal is to develop a novel chitosan endoluminal hemostatic dressing CEHD that is able to be delivered by a catheter to control and prevent prostatic bleeding via transurethral application enabling significant reduction in catheter indwelling time and providing for reduced length of hospital stay following prostatic surgery In our Phase I study we successfully demonstrated development of a safe and effective hemostatic chitosan CEHD for transurethral delivery incorporation of the CEHD as part of a urinary catheter device determination of transurethral operational procedures and protocols in deployment of the CEHD and demonstration of the feasibility of CEHD for hemorrhage control via transurethral application in a swine bladder neck injury model The Phase I study results demonstrated significant control of bleeding from bladder neck injury in the first hours with lower red cell counts in urine after the CEHD device deployment compared to controls in the in vivo model In the Phase II application through systematic final prototype improvements we propose to finalize the CEHD design and complete pre clinical efficacy and safety studies in support of an IDE application The proposed Phase II study includes modifications to the CEHD to enhance tissue adhesion and material dissolution finalization of the the CEHD to provide for manufacturability demonstration of ease of CEHD delivery demonstration of safety and efficacy in vivo PUBLIC HEALTH RELEVANCE The CEHD development will rapidly control bleeding and enable reduction in hospital days required for observation following prostatectomy As well as reducing discomfort associated with extended catheterization the CEHD development has the potential to significantly reduce the overall cost of hospitalization associated with bleeding following prostatectomy by hundreds of millions of dollars This development will reduce prostatectomy related morbidity and assist with reduction in mortality

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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