Clinical Trials Logo

Clinical Trial Summary

The study is a prospective randomized control trial consisting of subjects requiring ACL reconstruction with BTB autograft. Subjects were randomly divided into two groups following their inclusion in the study. One group underwent the normal ACL rehab protocol as determined by the participating surgeons. The study group underwent normal ACL rehab modified by use of a tourniquet for blood flow restriction during selected exercises.


Clinical Trial Description

On the day of the procedure, the surgeon will measure the subject's thigh circumference 1/3 distance from the superior pole of the patella to the inguinal crease. The subject will then undergo the normal BTB autograft ACL reconstruction procedure. A subject will be excluded from the study if a meniscal repair is performed. At the subject's two week post-operative clinic visit, the physician will measure thigh circumference at 1/3 distance from the superior pole of the patella to the inguinal crease. Study group subjects will begin physical therapy instructed BFR exercises at two weeks post operatively. Study group subjects will be taken through normal ACL rehab protocol as well as BFR exercises. Control group subjects will do the same exercises and formal physical therapy rehab protocol as the study group without BFR.

The BFR exercises will consist of: bilateral leg press week 3-10, eccentric leg press weeks 4-10, hamstring curl week 4-6, eccentric hamstring curl weeks 7-10, straight leg press weeks 6-10. The pressure used will be elevated to occluded blood flow by 80% (80% occlusion pressure) which will be determined for each individual subject. Subjects will do exercises at 20% of 1RM in 4 sets of 30-15-15-15 repetitions separated by 30 seconds of rest. Repetition maximum (1RM) will be determined by the contralateral leg, using the greatest amount of weight with full range of motion and proper form. This will be done over three separate tries, separated by one minute breaks. Resistance loads will be adjusted every 2 weeks as strength improves. During the exercise protocol, if patients are unable to complete the prescribed amount of repetitions, rest periods between sets will be increased as needed. The control group will do these exercises without BFR. Both study and control groups will also do the surgeons' standard post-ACL reconstruction physical therapy protocol.

Cuff pressures will be determined using the Loenneke et al outline, based off of thigh circumference and estimated cuff pressure for 50% artery occlusion [19].

Body composition (DEXA), bone density (DEXA), IKDC and Tegner Lysholm scores will be recorded at first rehabilitation visit, two weeks, eight weeks and 12 weeks following the initiation of rehab (1 wk following surgery). Y- balance, single leg squat distance, and single leg step down will be measured at 8 weeks and 12 weeks of rehab. Return to play will be recorded as the number of months after the day of operation until subject returns to sport. ;


Study Design


Related Conditions & MeSH terms

  • ACL Tear
  • Anterior Cruciate Ligament Injuries

NCT number NCT04484961
Study type Interventional
Source The Methodist Hospital System
Contact
Status Completed
Phase N/A
Start date March 18, 2016
Completion date July 10, 2020

See also
  Status Clinical Trial Phase
Completed NCT02450292 - Retrospective CT Imaging of BioComposite Interference Screw With BTB
Recruiting NCT05912777 - 3D Reconstruction of the Knee Based on MRI N/A
Recruiting NCT04058574 - Proprioceptive Isokinetic Repositioning, Functional Testing, and a Self-reported Questionnaire Before and After Anterior Cruciate Ligament Reconstruction N/A
Recruiting NCT06274008 - Exparel vs. ACB With Bupivacaine for ACL Reconstruction Phase 1
Active, not recruiting NCT05338385 - Readiness Outcomes Affecting Return to Sport 2.0: An Intervention Feasibility & Pilot Study N/A
Enrolling by invitation NCT05931627 - Tourniquet Use in Anterior Cruciate Ligament Repair N/A
Not yet recruiting NCT06340932 - Impact of Opioid Avoidance Protocol for ACL Reconstruction
Completed NCT05876013 - Reduced Knee Flexion Strength 18 Years After ACL Reconstruction in Hamstring Group Compared to Patellar Tendon Group
Recruiting NCT04748328 - Comparison Effectiveness Analysis Between ACL Reconstruction and Rehabilitation in Peripheral and Main Capital in Indonesia
Recruiting NCT04732585 - Kinematic Assessment of Human Peripheral Joints by Dynamic CT N/A
Completed NCT03243162 - Improving ACL Reconstruction Outcomes: CBPT N/A
Recruiting NCT06235736 - Do Patients With ACL Tears Demonstrate Weakness of the Soleus Muscle?
Not yet recruiting NCT06063915 - Isoinertial Rehabilitation in Recovering Hamstring Strength Following Surgical Anterior Cruciate Ligament Reconstruction N/A
Recruiting NCT04550299 - ACL Reconstruction With Simple and Double Bundle Technique Using Two Different Implants for Graft Fixation N/A
Not yet recruiting NCT04721119 - Comparing Adductor Canal Block and Adductor Canal Block-Local Infiltration Analgesia for Post-operative Pain Management N/A
Completed NCT04827264 - Safe Return to Play After ACL Reconstruction
Recruiting NCT04682392 - ACL Bone Health and Loading Study N/A
Recruiting NCT05241795 - Knee vs. Ankle Training on Knee Mechanics After ACLR N/A
Not yet recruiting NCT06096259 - Preventing Injured Knees From osteoArthritis: Severity Outcomes Phase 2
Not yet recruiting NCT05532189 - Anterior Cruciate Ligament (ACL) Reconstruction With Bone Tendon Bone Autograft With Versus Without Internal Bracing N/A