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: 1) development of a safe & effective hemostatic chitosan CEHD for transurethral delivery; 2) incorporation of the CEHD as part of a urinary catheter device; 3) determination of transurethral operational procedures and protocols in deployment of the CEHD; and 4) 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 3 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 1) modifications to the CEHD to enhance tissue adhesion and material dissolution; 2) finalization of the CEHD to provide for manufacturability; 3) demonstration of ease of CEHD delivery; and 4) demonstration of safety and efficacy in vivo.

Public Health Relevance

According to statistics from the department of Health & Human Service, there is an average 150,000 prostatic surgical procedures in US annually. Perioperative hemorrhage remains the major complication in these procedures which results in prolonged hospitalization. Prolonged indwelling urethera catheterization during the hospilzation causes significant patient discomfort and substantially increases healthcare cost. It is intended that the CEHD development will rapidly control bleeding and enable reduction in average 2-3 days hospital days required for observation following TURP to a single overnight stay. 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 TURP by hundreds of millions of dollars. PUBLIC HEALTH RELEVANCE: The CEHD development will rapidly control bleeding and enable reduction in average 2-3 days hospital days required for observation following TURP to a single overnight stay. 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 TURP by hundreds of millions of dollars. This development also will significantly reduce TURP related morbidity and assist with reduction in mortality

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Small Business Technology Transfer (STTR) Grants - Phase II (R42)
Project #
6R42DK078400-04
Application #
9352494
Study Section
Urologic and Genitourinary Physiology and Pathology (UGPP)
Program Officer
Kirkali, Ziya
Project Start
2007-04-01
Project End
2017-08-31
Budget Start
2016-04-15
Budget End
2017-08-31
Support Year
4
Fiscal Year
2015
Total Cost
$467,742
Indirect Cost
Name
Tricol Biomedical, Inc.
Department
Type
DUNS #
080240553
City
Portland
State
OR
Country
United States
Zip Code
97205