A Post-Market Clinical Evaluation of the Treatment of Femur Fractures with the Femoral Nail Greater Trochanter (GT) of the T2 Alpha Femur Antegrade GT/PF Nailing System

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Osteoarthritis
  • Age: Between 18 - 99 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Subject is a male or non-pregnant female age 18 years or older at the time of surgery;
    2. Subject is willing and able to give written informed consent and comply with the requirements of this Clinical Investigation Plan
    3. Subject is intended to be treated with the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System

You may not be eligible for this study if the following are true:

    1. Participants with active or suspected latent infection or marked local inflammation in or about the affected area
    2. Has compromised vascularity that would inhibit adequate blood supply to the fracture or the operative site
    3. Has documented bone stock compromised by disease, infection or prior implantation which cannot provide adequate support and / or fixation of the device
    4. Participants with documented or suspected sensitivity to materials
    5. Participants who are obese such that he / she produces a load on the implant which can lead to failure of fixation of the device or to failure of the device itself
    6. Has inadequate tissue coverage over the operative site.
    7. Has implant utilization that would interfere with anatomical structures or physiological performance
    8. Participants with mental or neuromuscular disorder which would create an unacceptable risk of fixation failure or complications in post-operative care
    9. Participants with any other medical or surgical condition which would preclude the potential benefit of surgery



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