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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06342063
Other study ID # 20-0070-E
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date January 31, 2024

Study information

Verified date March 2024
Source Women's College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective feasibility study is designed to assess pre-operative BFR in patients awaiting ACL reconstruction. This study will serve the following: (1) to determine if BFR improves strength testing prior to surgery and (2) to determine if BFR reduces QF muscle group atrophy prior to surgery. Additionally, preliminary results on pre-operative clinical and quality of life scores will be collected. If this study shows encouraging results, it will serve as a template for a more comprehensive randomized control trial.


Description:

Quadriceps femoris (QF) muscle function is an integral factor in the rehabilitation and overall outcome after lower extremity injury or surgical intervention. Atrophy of this muscle group is a common finding in patients undergoing anterior cruciate ligament (ACL) reconstruction. This is due to the immobility prior to surgery, vascular ischemia caused by a tourniquet intra-operatively and inability to perform high load strength training in the early post-operative period. A deficit in QF muscle strength can result in excessive joint loading and be a contributing factor in the early onset of osteoarthritis of the knee. It should be noted that a loss of strength in this primary knee extensor mechanism muscle group can persist for up to 2 years after surgery. Thus, the reduction of QF atrophy and maintenance of strength during an intervention such as an ACL reconstruction has large implications for the overall post-operative outcome and natural history of the knee joint. In order to combat the challenges of muscle atrophy for patients with an ACL injury, blood flow restriction (BFR) training has been shown to have beneficial effects in the post-operative period specifically. The process of using BFR therapy involves the application of an extremity tourniquet to occlude venous outflow and restrict arterial inflow. Thus, an anaerobic environment is created to promote muscle hypertrophy by having cells upregulate cell signalling, protein synthesis and ultimately myogenic proliferation. The use of BFR during lower extremity rehabilitation has shown that its simultaneous use with low load resistance training can have similar hypertrophic effects to isolated high load resistance training. This is ideal for patients who are initially unable to perform high intensity exercises shortly after an ACL reconstruction surgery, but are attempting to reduce overall QF atrophy. However, the use of BFR in the pre-operative period has yet to be well established. Preconditioning with an ischemic environment may provide an effective way to reduce QF atrophy with low load exercises while awaiting surgery. Additionally, having a period of sensitization with anaerobic conditions prior to surgery, may provide some resistance to the damaging effects of a tourniquet intra-operatively. The limited studies that have attempted to use BFR therapy prior to ACL surgery have had short intervention periods, small sample sizes and outcome variables that have not assessed overall clinical outcome. If BFR in the pre-operative setting can be shown to provide beneficial effects, it will be a valuable tool in maximizing the overall outcome of patients undergoing ACL reconstruction. This prospective feasibility study has been designed to assess pre-operative BFR in patients awaiting ACL reconstruction. This study will serve the following: (1) to determine if BFR improves strength testing prior to surgery and (2) to determine if BFR reduces QF muscle group atrophy prior to surgery. Additionally, preliminary results on pre-operative clinical and quality of life scores will be collected. If this study shows encouraging results, it will serve as a template for a more comprehensive randomized control trial.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date January 31, 2024
Est. primary completion date October 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Sagittal Knee instability caused by ACL tear requiring surgical reconstruction - Minimum 4 weeks since the time of injury - Age 18 to 50 years - Range of motion required ? Active extension deficit <5o, Active flexion > 120o - No previous surgery to affected knee Exclusion Criteria: - Functional impairment (neuro disease, gait abnormality, ambulatory aids at baseline) - Severe spine or lower limb injuries - Comorbidities including cardiovascular, respiratory or metabolic disease, blood coagulation disorders, current smoker

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Blood Flow Restriction Therapy
Patients wear a personalized tourniquet pressure system on their involved thigh while they perform a series of leg press machine exercises. This tourniquet is inflated.
Blood Flow Restriction Therapy Sham
Patients wear a personalized tourniquet pressure system on their involved thigh while they perform a series of leg press machine exercises. This tourniquet is not inflated.

Locations

Country Name City State
Canada Mount Sinai Hospital Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Women's College Hospital

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Wengle L, Migliorini F, Leroux T, Chahal J, Theodoropoulos J, Betsch M. The Effects of Blood Flow Restriction in Patients Undergoing Knee Surgery: A Systematic Review and Meta-analysis. Am J Sports Med. 2022 Aug;50(10):2824-2833. doi: 10.1177/03635465211027296. Epub 2021 Aug 18. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Biodex Strength Testing Quadriceps and Hamstring Muscle Strength and Endurance testing. Maximal peak torque (FT-LBS) was recorded for both knee flexion and extension at 60 degrees / second (indicative of strength) and 180 degrees / second (indicative of endurance). Baseline testing 1 day prior to physiotherapy initiation and Post intervention testing performed 1 day after physiotherapy completion but before ACL surgery.
Secondary Short Form Health Survey 12 (SF-12) Patient Reported Outcome Measure. Scores range from 0 to 100, with higher scores indicating better physical and mental health functioning. Baseline testing 1 day prior to physiotherapy initiation and Post intervention testing performed 1 day after physiotherapy completion but before ACL surgery.
Secondary Knee Injury and Osteoarthritis Outcome Score (KOOS) Patient Reported Outcome Measure. Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems. Baseline testing 1 day prior to physiotherapy initiation and Post intervention testing performed 1 day after physiotherapy completion but before ACL surgery.
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