Comparing rehabilitation methods after hip arthroscopy
Official title: Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation
Run by University of Colorado, Denver · NCT05165927 · Data updated 2026-11-12
This study tests whether adding blood flow restriction therapy to standard rehab helps people recover better after hip surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | University of Colorado, Denver Academic / other |
| Locations | 1 site (Englewood, Colorado) |
| Status | Recruiting |
| Started | April 29, 2022 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2025 |
| Registry record updated | December 11, 2024 |
| Trial ID | NCT05165927 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients with specific hip injuries such as labral tears or femoroacetabular impingement syndrome who are undergoing hip arthroscopy.
✕Probably not a fit
Patients with contraindications to BFR therapy or those undergoing bilateral hip surgeries within a short timeframe 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 study investigates the effectiveness of blood flow restriction (BFR) therapy in the rehabilitation process following hip arthroscopy. Participants will be randomly assigned to either a control group receiving standard rehabilitation or an intervention group that incorporates BFR therapy into their rehabilitation protocol. The treatment will last for 12 weeks, with follow-up assessments extending up to 2 years post-surgery. The study aims to evaluate the impact of BFR on recovery outcomes for patients with various hip injuries.
Why it matters
Potential benefit: If successful, this approach could enhance recovery and rehabilitation outcomes for patients undergoing hip arthroscopy.
How similar studies have gone: Previous studies have shown promising results with BFR therapy in rehabilitation, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients with labral tears, femoroacetabular impingement syndrome, loose bodies, ligamentum teres tears, and related intra-articular pathology to be treated with hip arthroscopy. Patients must also have access to a smartphone device in order to utilize the SAGA BFR application for use. The application is free to use. Exclusion Criteria: * bilateral hip surgeries to be performed within 12 weeks of each other, concomitant Peri-acetabular osteotomy, soft tissue repairs (hamstring, glute repairs), clinically diagnosed hip dysplasia, and the following BFR contraindications: * Deep Vein Thrombosis (DVT) * Pulmonary Embolism * Hemorrhagic/Thrombolytic Stroke * Clotting Disorders * Hemophilia or taking blood thinners * Pregnant or up to 6 months post-partum * Untreated Hypertension * Untreated Hypotension * Rhabdomyolysis or recent traumatic injury
Where it's running
-
UCHealth Steadman Hawkins Clinic Denver
Englewood, Colorado, United States Recruiting
Study contacts
- Principal investigator: James Genuario, MD — University of Colorado SOM
- Study coordinator: Lauren M Heylmun, BS
- Email: lauren.heylmun@cuanschutz.edu
- Phone: 7205169823
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Follow-up on outcomes after joint surgeries using Stryker devices
This study looks at how well Stryker devices work for people who have had shoulder, hip, or knee surgeries by checking their recovery and any issues they might have after 3 and 6 months.
-
Measuring muscle oxygen levels during recovery from knee and hip surgery
This study is testing a wearable sensor to see how well athletes recover from knee or hip surgery by measuring their muscle oxygen levels during physical therapy.
-
Creating a tool to improve CT imaging decisions for blunt trauma patients
This study is testing a new tool to help doctors decide when CT scans are really needed for patients with blunt trauma to avoid unnecessary radiation and costs.
-
Evaluating treatments for hip microinstability
This study is testing whether non-surgical physiotherapy or surgery works better for adults with hip microinstability to help improve their hip function.
-
Collecting data on Taperloc Complete stems for hip surgeries
This study is trying to see how safe and effective the Taperloc Complete hip implants are for people who have had hip surgery, by looking at both past patients and following new ones over the years.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.