Actively Recruiting
Single-Blind Randomized Clinical Trial of Concomitant Hip Arthroscopy During Periacetabular Osteotomy for Hip Dysplasia
Led by Mayo Clinic · Updated on 2025-09-05
106
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the outcomes of patients with hip dysplasia who undergo periacetabular osteotomy (PAO) surgery, comparing those who receive additional hip arthroscopy at the time of PAO with those who have PAO alone. The study aims to determine if adding intraarticular work during PAO improves pain and function, especially for patients with certain signs of joint damage or mechanical symptoms. This is a single-blind randomized clinical trial sponsored by Mayo Clinic. Participants are divided into two groups: one receives the standard PAO procedure on the day of surgery, and the other undergoes hip arthroscopy followed by PAO on the same day. Hip arthroscopy allows the surgeon to inspect and treat labral and cartilage issues, as well as correct abnormalities in the femoral head junction. The study focuses on patients aged 15 to 55 who have minimal or no arthritis and meet specific imaging criteria. During the study, researchers will assess participants using several outcome measures at one year after surgery, including scores for hip disability, osteoarthritis symptoms, activity levels, and functional ability. Participants will undergo standard preoperative imaging such as MRI arthrograms. The trial monitors pain, function, and activity outcomes to compare the benefits of adding hip arthroscopy to PAO surgery. The total participation and follow-up duration include assessments at one year post-operation.
CONDITIONS
Brief Title
Clinical Trial of Concomitant Hip Arthroscopy During PAO
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hip dysplasia electing periacetabular osteotomy for treatment
- Skeletally mature
- Age between 15 and 55 years
- Tonnis Grade 0 or 1 osteoarthritis (minimal or no arthritis)
- Ability to receive a standard preoperative MRI arthrogram of the hip
You will not qualify if you...
- Pregnant women
- Previous surgery about the hip
- Patients receiving PAO for acetabular retroversion without hip dysplasia
- Previous hip arthroscopy to address intra-articular pathology
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day (day of surgery)
Participants undergo periacetabular osteotomy surgery, with or without hip arthroscopy, depending on group assignment.
1 surgery visit (in-person)
Duration - Up to 1 year
Participants are followed to assess pain, function, and recovery after surgery.
Approximately 4 to 6 follow-up visits (in-person) over 1 year
Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
C
Cody Wyles, MD
L
Lauren Cole
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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