A Study Of Patient-Reported Outcomes Following Biceps Tenotomy

Overview

About this study

The purpose of this study is to evaluate patient-reported outcomes following biceps tenotomy, with a focus on functional outcomes, cosmetic concerns, satisfaction, pain relief, ongoing pain or spams, revision, decision-making and education during the entire process.

 

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:

  • Adults (≥18 years) who were treated conservatively for any bicep related pathology or who underwent surgical intervention with either bicep tenodesis or tenotomy of the LHB as an isolated or combined procedure at a single institution from 2019 to 2025 who can be reached for follow up, understand and respond in English (or translated version if applicable), and willing to provide informed consent.

Exclusion Criteria:

  • Revision procedures, patients under 18, arthroplasty procedures.  

 

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

 

Eligibility last updated 07/16/2025. 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

Jacksonville, Fla.

Mayo Clinic principal investigator

Erick Marigi

Contact us for the latest status

Contact information:

Erick Marigi

(904) 953-2496

Marigi.Erick@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20597387

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