Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
For general information about clinical research, read Learn About Studies.
Eligibility Criteria
- * Patient is 18 years of age or older.
- * Patient must have signed Institutional Review Board (IRB)/Ethics Committee (EC)-approved informed consent.
- * Patient is a candidate for primary or revision total elbow arthroplasty, based on symptoms including at least one of the following:
- * Elbow joint destruction which significantly compromises daily living activities
- * Post-traumatic lesions or bone loss contributing to elbow instability
- * Ankylosed joints, especially cases of bilateral ankylosis from causes other than active sepsis
- * Advanced rheumatoid arthritis, post-traumatic, or degenerative arthritis with incapacitating pain
- * Instability or loss of motion when the degree of joint or soft tissue damage precludes reliable osteosynthesis
- * Acute comminuted articular fracture of elbow joint surfaces that precludes less radical procedures, including 13-C3 fractures of the distal humerus
- * Patient is willing and able to complete scheduled follow-up evaluations as defined by the protocol.
- * Patient must have undergone a total elbow replacement with the Nexel system between July 2013 and the date of the site initiation visit.
- * Patient information available for each retrospective patient must, at minimum, include preoperative demographic information, preoperative physical exam information, the index surgery operative report, and details of the devices implanted.
- * Patient has a currently active or history of repeated local infection at the surgical site.
- * Patient has a current major infection distant from the operative site.
- * Patient has a history of prior sepsis.
- * Patient suffers from paralysis or dysfunctional neuropathy at the elbow joint.
- * Patient has significant ipsilateral hand dysfunction.
- * Patient has excessive scarring near the surgical site, which could prevent adequate soft tissue coverage.
- * Patient participates in daily activities that may cause significant stress to an implanted device such as heavy labor, torsional stress, and/or competitive sports.
- * Patient is a prisoner.
- * Patient is mentally incompetent or unable to understand what participation in the study entails.
- * Patient is a known alcohol or drug abuser.
- * Patient is anticipated to be non-compliant.
- * Patient is known to be pregnant.
Ages Eligible for Study
18 Years to
Sexes Eligible for Study
ALL
Accepts Healthy Volunteers
No