A Study Of Stryker Trauma & Extremities Shoulder Arthroplasty Devices

Overview

About this study

The purpose of this post-market retrospective data collection activity is to proactively generate post-market clinical follow-up performance and safety data on Stryker Trauma & Extremities Shoulder Arthroplasty Devices (“Products”) used in a real-world setting.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Data, from January 1st, 2023, will be collected by the Institution and Investigator from Pre-Operative, Operative/Discharge, and Standard of Care follow-up visits until the implant is removed or otherwise determined to be a failure.

Exclusion Criteria:

  • Less than 18 years of age.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 7/9/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Joaquin Sanchez-Sotelo

Open for enrollment

Contact information:

Kelly Sonsalla

(507) 293-3458

sonsalla.kelly@mayo.edu

Jacksonville, Fla.

Mayo Clinic principal investigator

Erick Marigi

Open for enrollment

Contact information:

Erick Marigi

(904) 953-2496

marigi.erick@mayo.edu

More information

Publications

Publications are currently not available