Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- Ottawa Hospital Research Institute
- Study ID
- NCT03481010
- Status
- Recruiting
Conditions
- Hip Dysplasia
Eligibility Criteria
- Sex
- ALL
- Age
- 16 Years - 50 Years
- Healthy Volunteers
- Not accepted
Interventions
- PAO with hip arthroscopy — PROCEDUREParticipants who are randomized to the Scope-PAO group will receive central compartment hip arthroscopy in addition to the PAO.
- PAO without hip arthroscopy — PROCEDUREParticipants who are randomized to the "PAO-only" group will receive a Bernese Periacetabular Osteotomy (PAO) for treatment of hip dysplasia.
Study Details
At present, it is not clear whether performing a hip arthroscopy at the same time as a PAO improves patient outcomes after surgery compared to a PAO alone. This research project will randomize patients to receive either a PAO alone, or a PAO and a hip arthroscopy at the same time.
Key Dates
- Start date
- Apr 4, 2018
- Status verified
- Dec 2025
- Primary completion
- Jul 31, 2030
- Completion
- Dec 31, 2030
Study Design
- Enrollment
- 204 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: PAO with hip arthroscopyPatient's in the "Scope PAO" group have been diagnosed with hip dysplasia and a decision has been made between the patient and the surgeon that the best way to treat the hip problems is with surgery. Patient's in the "Scope-PAO" group have been randomized to receive a periacetabular osteotomy with a hip arthroscopy.
- Active Comparator: PAO without hip arthroscopyPatient's in the "PAO-only" group have been diagnosed with hip dysplasia and a decision has been made between the patient and the surgeon that the best way to treat the hip problems is with surgery. Patient's in the "PAO-only" group have been randomized to receive a periacetabular osteotomy only.
Primary Outcome Measure
iHOT-33 [ Time Frame: 24 months ]
Central Contacts
- Geoffrey Wilkin, MD613-798-5555
- Cheryl Kreviazuk613-737-8920
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Northwestern University | Chicago | Illinois | 60611 | Michael Stover, MD |
| William Beaumont Hospital | Royal Oak | Michigan | 48073 | Ira Zaltz, MD |
| The Washington University | St Louis | Missouri | 63130 | John C. Clohisy, MD |
| Hospital for Special Surgery | New York | New York | 10021 | Ernest Sink, MD |
Find similar trials in Chicago, IL
Related Studies
- Pain Injection Versus Epidural Anesthesia for Hip Surgery in Pediatric Patients With Cerebral PalsyPHASE4 · Recruiting · University of California, Los Angeles · Los Angeles, California
- Early Feasibility Study of Cartilage Defect RepairRecruiting · Cytex Therapeutics, Inc. · St Louis, Missouri
- Clinical Trial of Concomitant Hip Arthroscopy During PAORecruiting · Mayo Clinic · Rochester, Minnesota
- Psychosocial Interventions for Young Adults With Hip PainNot Yet Recruiting · Michael C Willey · Iowa City, Iowa