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OsseoFit Stemless Shoulder System (Anatomic)

StatusEnrolling by Invitation
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Enrolling by invitation only Start date changed from estimate of Jul 2026 to Jul 23, 2026 · Eligibility criteria expanded, about 27 words · Secondary endpoints: details revised at 9 of 12 entries · 1 more Show 4 more changesShow less
    • Start date changed from estimate of Jul 2026 to Jul 23, 2026
    • Eligibility criteria expanded, about 27 words
    • Secondary endpoints: details revised at 9 of 12 entries
    • Site contacts updated at 1 of 2 sites
  2. Start date: Apr 2026 to Jul 2026 Study sites: 1 to 2v3 Show 1 more changeShow less
    • Study sites: 1 to 2
  3. Site contact updatedv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Zimmer Biomet
83 trials monitored
See 1 trial at risk
The purpose of this clinical research protocol is to evaluate the safety, efficacy, and long-term outcomes of the OsseoFit Stemless Shoulder System (Anatomic) in patients with a primary diagnosis of osteoarthritis. The study aims to assess the intraoperative characteristics, postoperative complications, functional outcomes, and radiographic findings associated with the use of the stemless implant system. Ultimately, this research aims to improve patient outcomes, enhance surgical techniques, and inform clinical decision-making in the treatment of shoulder pathology.
Trial Details
NCT Number NCT07421245
Lead Sponsor Zimmer Biomet
Conditions Shoulder Injuries, Shoulder Pain, Shoulder Fractures, Shoulder Arthritis, Shoulder Disease
Enrollment 136 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov