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Clinical Trials in France / NCT05926622
Recruiting Observational

Clinical and Radiological Outcomes of Medacta Shoulder System FR

NCT05926622 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-03-15
Last updated
2025-09-29

Condition(s) studied

Primary OsteoarthritisSecondary OsteoarthritisRotator Cuff Tear ArthropathyRheumatoid Arthritis ShoulderAvascular NecrosisFractureRevision of Shoulder Arthroplasty

Study summary

This is a post-marketing surveillance on Medacta Shoulder System

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinique Générale Annecy Annecy France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05926622 on ClinicalTrials.gov ↗ ← All trials in France