RecruitingNon-inflammatory Degenerative Joint DiseaseRhematoid ArthritisCorrection of Functional Deformity
Tornier Perform™ Reversed Monopost Study
Eligible age
18+ yrs
Accepts
All genders
Locations
2 states
Healthy volunteers
No
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About this study
This study is a Multi-center, Prospective Follow-up, Non-significant risk, Post-Market Clinical Follow-Up (PMCF) study to Evaluate the Safety and Effectiveness of the Tornier Perform™ Reversed MonoPost System.
Sponsor: Stryker Trauma and Extremities
You may qualify if…
- ✓ 18 years or older at the time of the informed consent.
- ✓ Informed and willing to sign an informed consent form (ICF) approved by Institutional Review Board (IRB) or Ethics Committee (EC).
- ✓ Willing and able to comply with the requirements of the study protocol
- ✓ Considered a candidate or having received shoulder arthroplasty with the device, having a functional deltoid muscle and with massive and non-repairable rotator cuff tear with pain disabled by:
- ✓ Rheumatoid arthritis
- ✓ Non-inflammatory degenerative joint disease (i.e. osteoarthritis and avascular necrosis)
- ✓ Correction of functional deformity
- ✓ Fracture of the Humeral Head
You may not qualify if…
- ✕ Contraindications or hypersensitivity to the use of the Tornier Perform™ Reversed MonoPost System or their components (e.g., metal sensitivity).
- ✕ Participation in the treatment period of another clinical trial during the clinical investigation.
- ✕ Any subject that meets the definition of a Vulnerable Subject per ISO 14155 Section 3.44. Examples include any subject "with lack of or loss of autonomy due to immaturity or through mental disability, persons in nursing homes, children, impoverished
Where it's recruiting
California
Rancho Mirage
Ohio
Columbus
Source: ClinicalTrials.gov · NCT07764614 · last updated 2026-10-23