RecruitingNot ApplicableNCT04113759

Blood Flow Restriction Following Hip Arthroscopy

Postoperative Blood Flow Restriction Training Following Hip Arthroscopy: A Randomized Clinical Trial


Sponsor

Rush University Medical Center

Enrollment

56 participants

Start Date

Aug 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This study will be a prospective randomized, double-blinded, placebo-controlled trial of patients undergoing primary hip arthroscopy for FAIS and/or labral pathology. All patients who sign the consent form will be enrolled in the study and randomized to one of the two treatment arms. Follow-up will take place at 1-month, 3-months, 6-months, and 1-year.


Eligibility

Min Age: 18 YearsMax Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a behavioral approach called Blood Flow Restriction Rehabilitative Therapy and a behavioral approach called Sham BFR Rehabilitative Therapy for people with femoral acetabular impingement and labral tear, glenoid. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 40 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALBlood Flow Restriction Rehabilitative Therapy

BFR cuffs placed at the proximal thigh, just inferior to the greater trochanter. Inflation time not to exceed 20 minutes. One BFR session per treatment. BFR exercise dosage: 4 sets of the following repetitions 30, 15, 15, 15, 30 second rest between sets, 1 min rest between exercises. Progress exercise if pain \<2/10 on VAS and RPE \<5 on 0-10 scale. (Heerey et al), and no break down in form.

BEHAVIORALSham BFR Rehabilitative Therapy

The schedule, type of exercises, repetition ranges, and other physical therapy interventions will be the same as the BFR experimental group - however a non-occlusive pressure will be applied with the cuff in the control group.


Locations(1)

Rush University Medical Center

Chicago, Illinois, United States

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NCT04113759


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