Blood Flow Restriction Training Following Glenoid Labral Repair
Withdrawn before enrolling · Not applicable
Conditions studied: Glenoid Labrum Tear
In brief
The objective of this study is to evaluate the effects of BFR training on patient reported outcome measures and shoulder muscle girth in patients following glenoid labral repair. The investigators hypothesize that participants receiving BFR with rehabilitation will have greater improvements in patient reported outcome measures and shoulder muscle girth than participants who are treated without BFR.
Key facts
- Study ID
- NCT03675620
- Run by
- Andrews Research & Education Foundation
- People needed
- 0
- Starts
- 2019-01-31
- Expected to finish
- 2022-12-07
- Last updated by the study team
- 2024-02-06
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Superior labrum anterior to posterior (SLAP) repair, anterior labral repair, anterior capsulorrhaphy, or posterior labral repair
- Willing to complete their post-operative rehabilitation at Andrews Institute Physical Therapy
You may not qualify if…
- Patients with prior procedures or significant injuries to the same shoulder will be excluded
- Patients with arthroscopic debridement of labral tears alone
- Patients with concomitant rotator cuff repair surgery
- Patients with Workers' Compensation or automobile insurance claim will be excluded.
- Patients who have a medical history involving any of the following medical conditions will be excluded - uncontrolled hypertension, diabetes, autoimmune disorders, rheumatoid or psoriatic arthritis, multiple sclerosis, peripheral vascular disease, peripheral neuropathy, deep vein thrombosis, pulmonary embolism, myocardial infarction, stroke, blood disorders, disorders requiring immunosuppression, cancer, an ongoing infectious disease, use of steroids, or significant cardiovascular, renal, hepatic or pulmonary disease
Where it is running
- Andrews Institute for Orthopaedics & Sports Medicine — Gulf Breeze, Florida, United States
Full record on ClinicalTrials.gov
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