Shoulder Innovations Clinical Data Registry
ConditionShoulder Arthroplasty
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShoulder Innovations
About this trial
The goal of this multi-center observational study is to collect long-term clinical outcome information for anatomic and reverse total shoulder arthroplasty (shoulder replacement).
Eligibility criteria
Qualifiers
At least 18 years of age.
Plan to receive or has received a shoulder arthroplasty surgical procedure, with a minimum of one implanted Shoulder Innovations (SI) device component and be willing and able to complete post-operative visits as long as at least one SI device component remains implanted.
Able to provide informed consent prior to enrollment in the study (unless a waiver has been obtained).
Agree to and be able to consistently answer the specified Patient Reported Outcome Measures (PROM) pre-operatively and at each of the post-operative visits without the use of a translator.
Disqualifiers
Participation in a clinical trial of an investigational drug or device that would confound the results of this trial. Participation in another observational registry is allowed provided there are no conflicting requirements to this trial.
Incarceration.
Any conditions, co-morbidities, restrictions, or obligations that would prohibit them from complying with the requirements of this study protocol.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Locations
8Alabama
St. Vincent's Orthopedics35205, Birmingham United States
St. Vincent's Orthopedics35205, Birmingham United States
California
California Pacific Orthopaedics94118, San Francisco United States
Colorado
Western Orthopaedics80222, Denver United States
Sponsors and collaborators
Shoulder Innovations
Lead sponsor
Source ClinicalTrials.gov