Comparing shoulder surgery techniques using ultrasound
Official title: Augmentation of Subscapularis Repair in Total Shoulder Arthroplasty
Run by Stanford University · NCT05487677 · Data updated 2026-11-12
This study is testing if using a special device called a Biobrace during shoulder surgery helps improve the repair compared to standard methods for people getting total shoulder replacements.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (Redwood City, California) |
| Status | Recruiting |
| Started | December 1, 2023 |
| Main results expected | September 1, 2028 |
| Study ends | December 1, 2030 |
| Registry record updated | August 19, 2026 |
| Trial ID | NCT05487677 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals scheduled for total shoulder arthroplasty.
✕Probably not a fit
Patients who are part of vulnerable populations or do not require shoulder surgery may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to compare the effectiveness of standard subscapularis tissue repair versus repair augmented with a Biobrace during total shoulder arthroplasty. The primary focus is on evaluating the images obtained through ultrasound to assess the quality of the repairs. Additionally, the study will investigate any clinical differences that may arise from using the Biobrace augmentation. The findings could lead to improved surgical techniques and better patient outcomes in shoulder surgeries.
Why it matters
Potential benefit: If successful, this study could enhance surgical outcomes for patients undergoing total shoulder arthroplasty.
How similar studies have gone: While there is ongoing research in shoulder surgery techniques, this specific approach using Biobrace augmentation is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Total Shoulder Arthroplasty Exclusion Criteria: * Vulnerable population
Where it's running
-
Stanford University
Redwood City, California, United States Recruiting
Study contacts
- Principal investigator: Michael T Freehill, MD — Stanford University
- Study coordinator: Jessica Nguyen
- Email: jessn16@stanford.edu
- Phone: 650-725-0003
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Single-shot nerve block with IV dexamethasone for rebound pain after shoulder surgery
This trial tests whether giving a one-time shoulder nerve block plus an IV dexamethasone dose can prevent rebound pain after shoulder surgery.
-
Using a serratus posterior superior intercostal plane block to reduce pain after arthroscopic shoulder surgery
This trial will test whether an ultrasound-guided serratus posterior superior intercostal plane block can reduce postoperative pain and opioid use for adults having arthroscopic shoulder surgery under general anesthesia.
-
Developing a kinesiophobia scale for shoulder injuries
This study is testing a new way to measure fear of movement in people with shoulder injuries to better understand how it affects their recovery.
-
Follow-up on outcomes after joint surgeries using Stryker devices
This study looks at how well Stryker devices work for people who have had shoulder, hip, or knee surgeries by checking their recovery and any issues they might have after 3 and 6 months.
-
Using a digital platform for home shoulder rehabilitation programs
This study tests if using a digital platform can help adults with shoulder problems stick to their home exercise programs and reduce the need for in-person therapy visits.
-
Comparing tendon repair options during reverse shoulder replacement
This study tests whether repairing a specific shoulder tendon during reverse shoulder replacement can help patients move their arm better and reduce the chance of dislocation.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.