SBIR/STTR Research Award

Microimaging System for Cancer Interventions

Award identifier b4937d4e5500e4ed49a2004ab90683cd9b51386ce0baeb5a1c7e647da2118df4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$89,801

Program and phase

SBIR · Phase I

Award year

2008

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
STERLING RESEARCH CORPORATION
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Sarcos Research Corporation proposes clinical testing of a system for minimally-invasive diagnostic and interventional procedures in cancer, using an image-guided interventional system based on the Sarcos- developed mic rocamera and a steerable microcatheter. In this project, we propose to: (7) design the system packaging for performing interventional procedures, and (7) collaborate with the physicians in the investigation of diagnostic and therapeutic options where acces s to small and difficult to reach anatomical spaces under direct visual control is critical to the success of the therapy as well as to minimizing trauma, recovery time, length of hospitalization, and the need for general anesthesia. The system: (7) addres ses the specific needs and constraints of minimally-invasive interventions that cannot be well met by conventional instrumentation, (7) increases safety of both minimally-invasive as well as traditional interventions by eliminating or minimizing the blind spots in the surgical field, (7) improves safety by enabling detailed visual observation of the operating field, (7) increases the availability of in-situ diagnostic procedures, (7) by virtue of disposability, eliminates current need for, and cost of end oscope cleaning and sterilizing, improving both patient's and operating personnel safety, (7) facilitates exploratory and diagnostic procedures, enabling earlier detection of disease and potentially earlier and less traumatic treatment. Initial clinical ap plications of the system will include otolaryngological procedures and examination of upper GIT. Phase 1 will result in prototype system development, laboratory characterization and the preparation of protocols for Phase 2 animal studies. Phase 2 will focu s on the fabrication of clinical prototypes, animal and pilot clinical studies, and the development of final product, leading to large scale clinical testing, regulatory clearance/approval, and commercialization.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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