A Study Of Clinical Outcomes Of Allograft Reconstruction Of The Lateral Collateral Ligament Complex Following Posterolateral Rotatory Instability

Overview

About this study

The purpose of this study is to evaluate the functional, clinical and surgical outcomes of patients who underwent allograft reconstruction of the LCLC following PLRI. This includes patients who have PLRI due to trauma or chronic lateral epicondylitis that is refractory to treatment. The primary objective is to evaluate postoperative outcomes, including patient-reported measures, complications, and objective stability.

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:

  • Patients who have undergone: Adults who have allograft reconstruction of the LCLC at Mayo Clinic

 

Exclusion Criteria:

  • Insufficient follow up data, patients who decline participation, patients with no history of trauma or lateral epicondylitis, patients with no PLRI prior to reconstruction, patients undergoing revision allograft LCLC

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

Eligibility last updated 03/30/2026. 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

Rochester, Minn.

Mayo Clinic principal investigator

Joaquin Sanchez-Sotelo, M.D., Ph.D.

Contact us for the latest status

More information

Publications

Publications are currently not available

Additional contact information

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