Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT05165927

Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation

Led by University of Colorado, Denver · Updated on 2024-12-11

120

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators plan to investigate the efficacy of blood flow restriction (BFR) therapy in post operative rehabilitation following hip arthroscopy. BFR has shown to be great at helping the recovery process. SAGA is a well-known smart training technology company, and the investigators aim to partner with SAGA to use the BFR cuffs as the intervention method. The BFR cuff will be added to the current SOC for hip scope PT for the intervention group.

CONDITIONS

Official Title

Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with labral tears, femoroacetabular impingement syndrome, loose bodies, ligamentum teres tears, or related intra-articular hip conditions to be treated with hip arthroscopy
  • Must have access to a smartphone device to use the free SAGA BFR application
Not Eligible

You will not qualify if you...

  • Bilateral hip surgeries scheduled within 12 weeks of each other
  • Concomitant peri-acetabular osteotomy or soft tissue repairs like hamstring or glute repairs
  • Clinically diagnosed hip dysplasia
  • Contraindications to BFR including Deep Vein Thrombosis, Pulmonary Embolism, Hemorrhagic or Thrombolytic Stroke, clotting disorders, hemophilia, or use of blood thinners
  • Pregnant or up to 6 months postpartum
  • Untreated hypertension or hypotension
  • Rhabdomyolysis or recent traumatic injury

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UCHealth Steadman Hawkins Clinic Denver

Englewood, Colorado, United States, 80012

Actively Recruiting

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Research Team

L

Lauren M Heylmun, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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