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Perform Humeral System Study

Abroad (travel likely)Recruiting

Conditions

Osteoarthritis Shoulder · Avascular Necrosis · Post-traumatic Arthrosis of Other Joints, Shoulder Region · Rotator Cuff Tear Arthropathy

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • Baptist Healthcare, Lexington, Kentucky, United States

    Contact: Study coordinator (Johnetta Comello) · johnetta.comello@bhsi.com
    Contact: Principal Investigator (Brent Morris)

  • Summit Orthopedics, Eagan, Minnesota, United States

    Contact: Study coordinator (Ned Tervola) · ntervola@gmail.com
    Contact: Principal Investigator (Michael Freehill, MD)

  • Mayo Clinic, Rochester, Minnesota, United States

  • Washington University, St Louis, Missouri, United States

  • Orthopedic Institute, Sioux Falls, South Dakota, United States

    Contact: Study coordinator (Khris Loe) · kloe@ortho-i.com
    Contact: Principal Investigator (Keith Baumgarten, MD)

  • University of Utah, Salt Lake City, Utah, United States

    Contact: Study coordinator (Ashley Neese) · Ashley.Neese@hsc.utah.edu
    Robert Tashjian (Sub-investigator)
    Contact: Principal Investigator (Christopher Joyce)

  • Roth McFarlane Hand and Upper Limb Centre, London, Ontario, Canada

  • Orthopedic Center Santy, Lyon, France

  • Schulthess Klinik, Zurich, Switzerland

  • Wrightington Hospital, Wigan, Lancashire, United Kingdom

Study leads

  • Rebecca Gibson

    Study Director

    Stryker Trauma

View source on ClinicalTrials.gov(opens in a new tab)