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Clinical and Radiological Outcomes of Medacta Shoulder System (BE)

Clinical and Radiological Outcomes of Medacta Shoulder System (BE)

Non Recruiting
18 years and older
All
Phase N/A

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Overview

This is a post-market surveillance study on Medacta Shoulder System

Eligibility

Inclusion Criteria:

  • Patients older than 18 years
  • Patient with one of the following diagnosis:
    1. Primary osteoarthritis
    2. Secondary osteoarthritis
    3. Cuff tear arthropathy; insufficient rotator cuff
    4. Acute fracture (<21d)
    5. Rheumatoid or inflammatory arthritis
    6. Avascular necrosis
    7. Other posttraumatic condition
    8. 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)

Study details
    Primary Osteoarthritis
    Secondary Osteoarthritis
    Rotator Cuff Tear Arthropathy
    Rheumatoid Arthritis Shoulder
    Avascular Necrosis
    Fracture
    Revision of Shoulder Arthroplasty

NCT05002335

Medacta International SA

21 October 2025

FAQs

Learn more about clinical trials

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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