SBIR/STTR Research Award

Chitosan Gastrointestinal Hemostatic Dressing

Award identifier 0b53bce0268b77e0b0454ed36078a3c27167ea3542e311a67fb8a77c85d802f7Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$919,507

Program and phase

SBIR · Phase II

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
TRICOL BIOMEDICAL, INC
Proposal award date
2018-04-11
Contract end date
2021-03-31
UEI
JG5HB91R2FB4
Solicitation number
PA17-302
Topic code
200

Research abstract

AbstractSerious non variceal upper gastrointestinal bleedingNVUGIBis a major cause of morbidity and mortality worldwideIncidence of NVUGIB in the US is close toevents peradultswith approximatelyhospital admissions annuallyUS treatment and prevention of NVUGIB continues to be a major medical emergencycostingmillion dollars every yearFailure in standard of care for NVUGIB results in mortality rates fromin the USAn improved hemostatic approach to NVUGIB will significantly reduce hemorrhage related morbidity and mortality with reduced cost of hospital careThe ideal device would be nontoxicable to be stored foryears without refrigerationbe easily deployedprovide immediate hemostasis for difficult to control brisk andamppulsatile bleedingallow successful low accuracy acuity placement in a bleeding obscured surgical fieldnot require significant follow up or removaland dissolve or be digested in the gastric cavity in underdaysThis proposal addresses finalization in development of such a deviceTo address serious NVUGIBTricol Biomedical andampOregon Health andampScience University propose to finalize development of a foldablehighly efficaciouschitosan gastrointestinal hemostatic dressingCGHDwith wire deliveryWDvia a standard endoscope working channelThe primary objective of this research proposal is to complete development of a novel efficacious CGHD DW and its management of challenging acute GI bleeding in the gastric environment that can be left in place to be fully digested or dissolved in less thanhoursThe final CGHD WD device will be validated in aday study of a large animal model of briskpulsatile UGIB to support an investigational device exemptionIDEfor a Phase I clinical studyThe central hypothesis of this Phase II proposal is that the finalized CGHD DW with delivery through the standard endoscope working channel will provide effectiveimmediate and sustained hemostasis for brisk NVUGIB NarrativeSerious non variceal upper gastrointestinal bleedingNVUGIBis a major cause of morbidity and mortality worldwide with incidence of NVUGIB in the US close toevents peradultswith approximatelyhospital admissions annuallyThe chitosan gastrointestinal hemostatic dressingCGHDdelivered by wireWDvia the working channel of a standard endoscope will provide for rapid deployment of an advancedtissue adherenthemostatic dressing to provide immediate hemostasis for difficult to control NVUGIB and allow for successful low accuracy acuity placement in an obscured surgical field without need for significant follow up or removalThe successfully completed CGHD DW device will significantly reduce NVUGIB hemorrhage related morbidity and mortality with reduced cost of hospital care

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

2 SBIR/STTR records share this UEI (2018–2021). Reported award amounts total $1,773,365. Reported amounts are not federal obligations.

Phases: Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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