A Repositionable Tissue Anchor for Osteoporortic Bone

Information

  • Research Project
  • 6803573
  • ApplicationId
    6803573
  • Core Project Number
    R44AR050380
  • Full Project Number
    5R44AR050380-03
  • Serial Number
    50380
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/2001 - 23 years ago
  • Project End Date
    8/31/2007 - 17 years ago
  • Program Officer Name
    PANAGIS, JAMES S.
  • Budget Start Date
    9/2/2004 - 20 years ago
  • Budget End Date
    8/31/2007 - 17 years ago
  • Fiscal Year
    2004
  • Support Year
    3
  • Suffix
  • Award Notice Date
    8/31/2004 - 20 years ago
Organizations

A Repositionable Tissue Anchor for Osteoporortic Bone

[unreadable] DESCRIPTION (provided by applicant): Suture anchors provide a quick, secure, and simple means of surgically attaching soft tissue to bone. Since their introduction in 1985, suture anchors have been widely used in a variety of surgical procedures. They provide a significant savings in time and cost to both surgeon and patient. However, there are a number of shortcomings with current anchors. Existing suture anchors perform poorly in osteoporotic bone and cannot be repositioned easily following implantation. The issue of attachment to osteoporotic bone will become increasingly important with a growing active adult population. We propose the development of a novel, new suture anchor technology that possesses the same benefits of existing devices but yields significant advantages. The new anchor is less invasive, can be readily repositioned, provides exceptional performance in poor quality bone, and can be used as a revision device for other anchors. Based on the Phase I confirmation of feasibility, the goal of the Phase II work is the specific product development of the rotator cuff repair anchor, followed by design modification for a diverse product line of anchor products. Rotator cuff repair is a high volume surgical operation that often involves poor quality bone in the proximal humerus where standard anchor devices do not provide adequate fixation strength. The development of this anchor and associated insertion tooling will utilize a finite element analysis design tool. A thorough bench testing regimen will be performed to establish regulatory equivalence to a commercial predicate device, with a special focus on fixation strength in an osteoporotic bone model. A group of shoulder specialists will assess the utility of the anchor system by performing simulated cuff repairs in a cadaveric model. Rotator cuff reconstructions using the prototype systems and current devices will also be tested in a dynamic shoulder testing system to evaluate the cyclic failure risk of early rehabilitation protocols. Many references in the literature that indicate that early, aggressive rehabilitation regimens may cause a significant decrease in anchor fixation strength, laxity in the cuff reconstruction, and even the elevated failure rate of the operation. A review panel of surgeons in a diverse range of specialties will contribute specifications in the development process and critically review the system design and final project results. [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES
  • Activity
    R44
  • Administering IC
    AR
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    562610
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    846
  • Ed Inst. Type
  • Funding ICs
    NIAMS:562610\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ELECTROSONICS MEDICAL INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CLEVELAND
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    44114
  • Organization District
    UNITED STATES