What this study is
The study will assess the outcomes of patients treated with concomitant hip arthroscopy at the time of periacetabular osteotomy (PAO) for patients with hip dysplasia compared with patients treated with PAO alone.
What's being tested
- Periacetabular osteotomy
Intervention · PROCEDURE
The Bernese periacetabular osteotomy has become the osteotomy of choice in North America for correction of the dysplastic hip. The ability to position the acetabular component in a specifically desired position for each individual patient improves joint biomechanics, restores joint balance and stability, and offloads the structures at risk for damage such as the labrum and the adjacent articular cartilage.
- Periacetabular osteotomy with hip arthroscopy
Intervention · PROCEDURE
An intraarticular assessment with hip arthroscopy (HA) at the time of periacetabular osteotomy allows the surgeon to assess and treat the associated labral and chondral pathology and allows the surgeon to treat abnormalities of the femoral head junction.
Study details
- Official title
- Single-Blind Randomized Clinical Trial of Concomitant Hip Arthroscopy During Periacetabular Osteotomy for the Management of Hip Dysplasia
- Sponsor
- Mayo Clinic
- Conditions
- Hip Dysplasia
- Enrolling
- 106 people
- Starts
- 2017-08-23
- Est. completion
- 2028-06
- Design
- Single-blind, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 15 Years – 55 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Diagnosis of hip dysplasia (DDH) electing periacetabular osteotomy (PAO) for treatment
- Skeletally mature
- Age 15 - 55
- Tonnis Grade 0 or 1 osteoarthritis (minimal or no arthritis)
- Ability to receive a standard of care preoperative (magnetic resonance imaging) MRI arthrogram of the hip
You can't join if
- Pregnant women
- Previous surgery about the hip
- Patients receiving PAO for acetabular retroversion in the absence of DDH
- Previous hip arthroscopy to address intra-articular pathology
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openMayo Clinic
Rochester, Minnesota, United States
- Cody Wyles, MD · Contact(507) 284-1175wyles.cody@mayo.edu
- Rafael Sierra, MD · Principal investigator
Recruiting
Study team
Sponsor
Mayo Clinic
Study ID 17-001014
Principal investigator
Rafael Sierra, MD
Mayo Clinic
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.