Subscapularis Repair Augmentation for Total Shoulder Arthroplasty

Recruiting N/A Interventional Study
Shoulder Injuries
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
100 (estimated)
Sponsor
Stanford University · Other
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About This Trial

The primary purpose of this research is to compare the images obtained by ultrasound between a standard repair of the subscapularis tissue and after repair with a Biobrace. The secondary purpose is to determine if there are any clinical differences.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Total Shoulder Arthroplasty Exclusion Criteria: * Vulnerable population
Contacts

Jessica Nguyen

650-725-0003

jessn16@stanford.edu

CONTACT