Comparison of Outcomes Between Biceps Tenotomy and Tenodesis in the Treatment of the Long Head of the Biceps Pathology

Not Applicable

Completed

• Conditions: Chronic Refractive Bicipital Pain
• Interventions: Procedure: Biceps tenotomy; Procedure: Biceps tenodesis

• Registration Number: NCT02107586
• Lead Sponsor: University of Chicago

Brief Summary

The purpose of the study is to determine what the different outcomes are for biceps tenodesis and tenotomy in the treatment of the long head of the biceps pathology.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2013-05-13
• Study First Submitted: 2014-04-04
• Study First Submitted QC: 2014-04-07
• Primary Completion: 2014-04-08
• Study Completion: 2014-04-08
• Study First Posted: 2014-04-08
• Status Verified: 2023-04
• Last Update Submitted: 2023-04-24
• Last Update Posted: 2023-04-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

• patient with chronic refractive bicipital pain

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Exclusion Criteria

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Biceps tenotomy	Biceps tenotomy	32 subjects in the study will receive biceps tenotomy as a surgical intervention
Biceps tenodesis	Biceps tenodesis	32 subjects in the study will receive biceps tenodesis as a surgical intervention

Primary Outcome Measures

Name	Time	Method
American Shoulder and Elbow Surgeons (ASES) Shoulder Score	one year	The scale measures pain from 0 to 10 and also includes a questionnaire for assessing the activity of daily living.

Secondary Outcome Measures

Name	Time	Method
EuroQol EQ-5D	one year	The questionnaire measures mobility, ability to care for self, ability to perform usual activities, pain/discomfort, and anxiety/depression

Trial Locations

Locations (1)

University of Chicago Medical Center; 🇺🇸 Chicago, Illinois, United States