OsseoFit Stemless Shoulder System (Anatomic)

Part of paid clinical trials in Buffalo, New York.

Sponsor
Zimmer Biomet
Study ID
NCT07421245
Status
Not Yet Recruiting

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Conditions

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

Eligibility Criteria

Sex
ALL
Age
20 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • OsseoFit Stemless Inlay — DEVICE
    Inlay implants have a dished superior portion with a shorter fin length to allow the implant to sit within the bone.
  • OsseoFit Stemless Onlay — DEVICE
    The Onlay implants sit on top of the prepared bone.

Study Details

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.

Key Dates

Start date
Apr 30, 2026
Status verified
Apr 2026
Primary completion
Jan 31, 2036
Completion
Jan 31, 2036

Study Design

Enrollment
136 participants (estimated)

Arms

  • Arm: OsseoFit Stemless Inlay
    Subjects who were implanted with the Inlay variant of the Osseofit Stemless Shoulder System.
  • Arm: OsseoFit Stemless Onlay
    Subjects who were implanted with the Onlay variant of the Osseofit Stemless Shoulder System.

Primary Outcome Measure

the American Shoulder and Elbow Surgeons (ASES) Shoulder Score [ Time Frame: 2 years ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The Research Foundation for the State University of New YorkBuffaloNew York14228-

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