New shoulder implant tested for severe arthritis – but study halted early

NCT ID NCT02204228

First seen Oct 31, 2025 · Last updated Jun 23, 2026 · Updated 26 times

Summary

This study looked at the TITAN Reverse Shoulder System, a device used to replace the shoulder joint in people with severe arthritis and a torn rotator cuff. The goal was to see if it relieves pain and improves movement. About 151 people were planned to take part, but the study was stopped early, so the full results are not available.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Active Orthopedics

    Glen Ridge, New Jersey, 07028, United States

  • Barts Health NHS Trust

    London, United Kingdom

  • Clinique Bizet

    Paris, France

  • Hospital de Manacor - Llevant

    Manacor, 07500, Spain

  • Hospital of the University of Pennsylvania

    Philadelphia, Pennsylvania, 19104, United States

  • Johns Hopkins University

    Columbia, Maryland, 21044, United States

  • Mississipi Bone and Joint Clinic

    Starkville, Mississippi, 39759, United States

  • The Rothman Institute

    Philadelphia, Pennsylvania, 19107, United States

  • University of Florida

    Gainesville, Florida, 32607, United States

  • Westphal Orthopaedics

    Lancaster, Pennsylvania, 17601, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

TITAN™ Reverse Shoulder System (a shoulder replacement device)

What this could lead to

If successful, this device could provide a reliable option for pain relief and improved shoulder function in patients with severe arthritis and a torn rotator cuff.

What could go wrong

The study was terminated early, so results are limited. As with any surgery, risks include infection, implant loosening, or nerve injury.

Conditions

The condition(s) this trial relates to.

bone fracture osteoarthritis osteonecrosis rheumatoid arthritis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.