Development of a lightweight, portable, pneumatic drive unit for long term counterpulsationsupport

Information

  • Research Project
  • 9847032
  • ApplicationId
    9847032
  • Core Project Number
    R43HL149528
  • Full Project Number
    1R43HL149528-01
  • Serial Number
    149528
  • FOA Number
    PA-18-574
  • Sub Project Id
  • Project Start Date
    7/1/2019 - 6 years ago
  • Project End Date
    12/31/2019 - 5 years ago
  • Program Officer Name
    LEE, ALBERT
  • Budget Start Date
    7/1/2019 - 6 years ago
  • Budget End Date
    12/31/2019 - 5 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    6/25/2019 - 6 years ago
Organizations

Development of a lightweight, portable, pneumatic drive unit for long term counterpulsationsupport

ABSTRACT Heart failure (HF) rapidly progresses despite optimal medical management and cardiac resynchronization therapy. Left ventricular assist devices are reserved only for end-stage HF due to surgical invasiveness. Long- term mechanical circulatory support options for less sick heart failure patients (Class III, early Class IV), which may slow down or reverse HF progression, are limited. To fulfill this therapeutic gap, NuPulseCV (Raleigh, NC) is developing a chronic implantable counterpulsation system (iVAS) to treat HF patients. The NuPulseCV system has been developed for less invasive implantation in the descending aorta without the need to enter the chest and enables complete patient mobility. In an ongoing Food and Drug Administration (FDA) approved clinical study, the iVAS was successfully implanted in over 50 patients and improved patient hemodynamics as evidenced by statistically significant improvements in cardiac index (39%), ejection fraction (48%), and cardiac power index (35%) over baseline values. However, the first-generation NuPulseCV drive unit (NDU) used for the clinical studies is a feasibility model that is not durable, expensive to manufacture, bulky, and not ergonomic, limiting patient mobility and ambulatory use. In this SBIR Phase I study, we will demonstrate feasibility of a durable, light-weight and ergonomic second-generation NDU to provide effective counterpulsation support. This objective will be accomplished by (1) fabrication of the second generation NDU using previously identified components to reduce size, weight, noise, and improving NDU performance, (2) demonstrating feasibility using mock loop, and acute and chronic ovine models. Results from the SBIR Phase I study will be used for optimization of the NDU during SBIR Phase II, which will then lead to an FDA submission for a pivotal study. The program detailed in this proposal leverages the engineering expertise and development work of NuPulseCV guided by an innovative group of physicians at Duke University (Durham, NC). Our long-term objective is to successfully introduce the portable and ergonomic NuPulseCV system into the clinical setting as a long-term counterpulsation therapy to treat heart failure patients with minimal adverse events and help restore their quality of life.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R43
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    224999
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:224999\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NUPULSECV, INC.
  • Organization Department
  • Organization DUNS
    085882332
  • Organization City
    RALEIGH
  • Organization State
    NC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    276074163
  • Organization District
    UNITED STATES