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OsseoFit Stemless Shoulder System (Anatomic)

NCT07421245 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 136

Last updated 2026-07-09

No results posted yet for this study

Summary

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.

Conditions

  • Shoulder Injuries
  • Shoulder Pain
  • Shoulder Fractures
  • Shoulder Arthritis
  • Shoulder Disease

Interventions

DEVICE

OsseoFit Stemless Inlay

Inlay implants have a dished superior portion with a shorter fin length to allow the implant to sit within the bone.

DEVICE

OsseoFit Stemless Onlay

The Onlay implants sit on top of the prepared bone.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Jim Nevelos · Zimmer Biomet

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2036-01-31
Completion
2036-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07421245 on ClinicalTrials.gov