Zimmer Biomet Shoulder Arthroplasty PMCF Study
This trial has no sites in United States.
It has sites in 2 countries. Choose a country to see its sites.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Zimmer Biomet
- Trial code
- NCT06920459
- Record updated
- 8 June 2026
- Original description
This is a multicenter, prospective, non-controlled post market surveillance study. The objectives of this study are to confirm the safety, performance, and clinical benefits of the Zimmer Biomet Shoulder Arthroplasty systems in primary anatomic shoulder arthroplasty and its instrumentation. Safety of the systems will be assessed by monitoring the frequency and incidence of adverse events. The performance and clinical benefits will be evaluated by assessment of the overall pain and functional performance, qualify of life, and radiographic parameters of all enrolled study subjects.Read full original descriptionShow less
Zimmer Biomet Shoulder Arthroplasty Long-term Post Market Clinical Follow-up Study
This is a multicenter, prospective, non-controlled post market surveillance study. The objectives of this study are to confirm the safety, performance, and clinical benefits of the Zimmer Biomet Shoulder Arthroplasty systems in primary anatomic shoulder arthroplasty and its instrumentation. Safety of the systems will be assessed by monitoring the frequency and incidence of adverse events. The performance and clinical benefits will be evaluated by assessment of the overall pain and functional performance, qualify of life, and radiographic parameters of all enrolled study subjects.
Inclusion: Patient must be 20 years of age or older; Patient must be anatomically and structurally suited to receive shoulder arthroplasty implants; Patient is a candidate for shoulder arthroplasty due to one or more of the following:; Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis; Rheumatoid arthritis. Fractures of the proximal humerus, where other methods of treatment are deemed inadequate; Difficult clinical management problems, where other method of treatment may not be suitable or may be inadequate; Patient must be able and willing to complete the protocol required follow-up; Patient must be able and willing to sign the IRB/EC approved informed consent.
Exclusion: Patient is a vulnerable subject (prisoner, mentally incompetent or unable to understand what participation to the study entails, a known alcohol or drug abuser, and/or anticipated to be non- compliant); Patient has any condition which would in the judgement of the Investigator, place the patient at undue risk or interfere with the study; Patient is uncooperative or patient with neurologic disorders who is incapable or unwilling to follow directions; Patient has any sign of infection affecting the shoulder joint or in its proximity which may spread to the implant site; Patient has any neuromuscular disease compromising the affected limb that would render the procedure unjustifiable; Patient has a metabolic disorder that may impair bone formation; Patient is unwilling or unable to give consent or to comply with the follow-up program; Patient is known to be pregnant or breastfeeding; Patient has rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram; Patient presents with osteoporosis, which in the opinion of the Investigator, may limit the subject's ability to support total shoulder arthroplasty using the study device; Patient has osteomalacia.