This study is a multicenter, prospective, non-controlled post market clinical follow-up study. The objectives of this study are to confirm the safety and performance of the commercially available Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion Criteria:
* Patient is 18 to 75 years of age, inclusive.
* Patient is skeletally mature.
* Patient qualifies for primary unilateral or simultaneous bilateral total hip arthroplasty (THA) based on physical exam and medical history including at least one of the following:
* Osteoarthritis
* Avascular necrosis (AVN)
* Inflammatory arthritis
* Rheumatoid arthritis with adequate bone quality
* Post-traumatic arthritis
* Congenital hip dysplasia.
* Patient has no history of previous total hip replacement or arthrodesis of the affected hip joint(s). Patient has a Harris Hip Score \<70 in the affected hip and a Harris Hip pain rating of moderate, marked, or disabled.
* Patient is willing and able to provide written informed consent.
* Patient is willing and able to cooperate in the required post-operative therapy.
* Patient is willing and able to complete scheduled follow-up evaluations as described in the Informed Consent.
* Patient has participated in the Informed Consent process and has signed the Ethics Committee approved informed consent.
Exclusion Criteria:
* The patient is:
* A prisoner
* Mentally incompetent or unable to understand what participation in the study entails.
* A known alcohol or drug abuser
* Anticipated to be non-compliant
* The patient has a neuromuscular disorder, vascular disorder or other condition that could contribute to prosthesis instability, prosthesis fixation failure, or complications in postoperative care.
* The pa…
What they're measuring
1
Implant survival based on removal or intended removal of the device and determined using the Kaplan-Meier method