Status:
WITHDRAWN
BFR After Biceps Tendon Repair and MPFLR
Lead Sponsor:
Mayo Clinic
Conditions:
Patellofemoral Joint Dislocation
Bicep Tendon Rupture
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The purpose of this study is to examine the effect of utilizing blood flow restriction (BFR) therapy after distal biceps tendon repair or medial patellofemoral ligament reconstruction (MPFLR) followin...
Eligibility Criteria
Inclusion
- Subjects will be recruited from our ambulatory sports medicine clinics. We will include patients aged 18-80 who suffered a biceps tear and are undergoing biceps repair or MPFLR
Exclusion
- Subjects will be excluded if they are undergoing revision biceps repair or revision MPFLR, history of DVT, neurovascular injury, unable to tolerate BFR treatment, unable to complete physical therapy, peripheral vascular disease
- Subjects will be withdrawn from the study if they are unable to tolerate the BFR therapy. Additionally if they suffer from any complications of the therapy they will be withdrawn immediately. This will be facilitated by describing the reasons for withdrawal to the patient prior to initiating the study and ask patients and other providers to inform the investigators if there are any issues or concerns.
Key Trial Info
Start Date :
July 29 2025
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 29 2025
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT05375071
Start Date
July 29 2025
End Date
July 29 2025
Last Update
September 29 2025
Active Locations (1)
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1
Mayo Clinic Rochester
Rochester, Minnesota, United States, 55902