Clinical trial Recruiting at 1 site Interventional Ages 18 to 40

Blood flow restriction therapy after hip surgery

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

Run by Rush University Medical Center · NCT04113759 · Data updated 2026-11-12

This study is testing if a special therapy that restricts blood flow can help people recover stronger and faster after hip surgery for certain injuries.

Quick facts

Study typeInterventional
Ages18 Years to 40 Years
SexAll
Enrollment56 (estimated)
SponsorRush University Medical Center
Academic / other
Locations1 site (Chicago, Illinois)
StatusRecruiting
StartedAugust 1, 2023
Main results expectedNovember 2027
Study endsJanuary 2028
Registry record updatedDecember 5, 2025
Trial IDNCT04113759 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking adults aged 18-40 scheduled for primary hip arthroscopy due to labral pathology or femoral acetabular impingement.

Probably not a fit

Patients over 40, those with prior hip or knee surgeries, or individuals with certain medical conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of blood flow restriction (BFR) therapy in enhancing muscle growth and strength recovery in patients undergoing hip arthroscopy for femoral acetabular impingement and labral tears. Participants will be randomly assigned to receive either BFR therapy or a sham treatment, with their progress monitored through strength testing, leg measurements, and MRI assessments over a year. The study aims to determine if BFR can improve rehabilitation outcomes compared to standard recovery methods.

Why it matters

Potential benefit: If successful, this approach could lead to improved muscle recovery and rehabilitation outcomes for patients after hip arthroscopy.

How similar studies have gone: Other studies have shown promising results with blood flow restriction therapy in various rehabilitation settings, suggesting potential for success in this novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patients 18-40
* English-speaking
* Clinical and radiographic examination (MRI) consistent FAIS and/or labral pathology, and are schedule for primary hip arthroscopy
* Written and informed consent for study participation

Exclusion Criteria:

* Patients younger than 18 or older than 40 years of age
* Non-native English speaker
* Revision surgery or prior history of ipsilateral hip or knee surgery
* Inability to comply with the proposed follow-up clinic visits
* Patients lacking decisional capacity
* Patients with a history of deep vein thrombosis, pulmonary embolism, or known clotting disorder or hypercoagulable state
* Pregnant or breast-feeding women. Pregnancy as determined by a positive pregnancy test prior to procedure. Females of childbearing potential must agree to use an acceptable birth control method during study participation.
* Worker's compensation patients
* Any clinically significant finding that would place the patient at health risk, impact the study, or affect the completion of the study
* Any psychiatric illness that would prevent comprehension of the details and nature of the study and interfere with follow-up clinic visits

Where it's running

  • Rush University Medical Center
    Chicago, Illinois, United States
    Recruiting

Study contacts

  • Principal investigator: Jorge Chahla, MD PhD — Rush University Medical Center
  • Study coordinator: Carla M. Edwards, PhD
  • Email: carla_edwards@rush.edu
  • Phone: 312-563-5735

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.