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Augmentation of Subscapularis Repair in Total Shoulder Arthroplasty
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.
The investigators would like to learn if subscapularis repair augmentation with the Biobrace in total shoulder arthroplasty (reverse and anatomic) will result in sonographic and/or clinical improvements. This will allow for improvements in technique and better outcomes for patients going forward.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Stanford University
Redwood City, California, United States
Start Date
December 1, 2023
Primary Completion Date
September 1, 2026
Completion Date
December 1, 2028
Last Updated
March 3, 2026
100
ESTIMATED participants
BioBrace Augmentation
DEVICE
Standard Repair with Sutures
PROCEDURE
Lead Sponsor
Stanford University
NCT06320925
NCT06572696
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04003311