Clinical and Radiological Outcomes of Medacta Shoulder System FR

Recruiting · NCT05926622 · Observational (researchers observe without assigning treatment) · Lead sponsor: Medacta International SA

What this trial is about

This is a post-marketing surveillance on Medacta Shoulder System

Age range

18 Years and older

Sex

All (male and female)

Healthy volunteers

No - a diagnosis or condition is required

Phase

Not specified

Study type

Observational (researchers observe without assigning treatment)

Patients older than 18 years
Patient with one of the following diagnosis:
Primary osteoarthritis Secondary osteoarthritis Cuff tear arthropathy; insufficient rotator cuff Acute fracture (\<21d) Rheumatoid or inflammatory arthritis Avascular necrosis Other posttraumatic condition Revision of shoulder arthroplasty

Patients with malignant diseases (at the time of surgery)
Patients with proven or suspect infections (at the time of surgery)
Patients with functional deficits other than dysfunction of the shoulder (at the time of surgery)
Patients with known incompatibility or allergy to products materials (at the time of surgery)

1 location listed.