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:
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Conditions: Osteoarthritis
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Age: Between 18 Year(s) - 99 Year(s)
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Gender: Male or Female
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Other Inclusion Criteria:
- Subject is a male or non-pregnant female age 18 years or older at the time of surgery;
- Subject is willing and able to give written informed consent and comply with the requirements of this Clinical Investigation Plan
- 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:
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- Participants with active or suspected latent infection or marked local inflammation in or about the affected area
- Has compromised vascularity that would inhibit adequate blood supply to the fracture or the operative site
- Has documented bone stock compromised by disease, infection or prior implantation which cannot provide adequate support and / or fixation of the device
- Participants with documented or suspected sensitivity to materials
- 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
- Has inadequate tissue coverage over the operative site.
- Has implant utilization that would interfere with anatomical structures or physiological performance
- Participants with mental or neuromuscular disorder which would create an unacceptable risk of fixation failure or complications in post-operative care
- Participants with any other medical or surgical condition which would preclude the potential benefit of surgery
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.