Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology

Description

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.

Conditions

Hip Dysplasia

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Study Overview

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Study Details

Study overview

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.

Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology: A Multicenter Randomized Controlled Trial

Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology

Condition
Hip Dysplasia
Intervention / Treatment

-

Contacts and Locations

Chicago

Northwestern University, Chicago, Illinois, United States, 60611

Royal Oak

William Beaumont Hospital, Royal Oak, Michigan, United States, 48073

Saint Louis

The Washington University, Saint Louis, Missouri, United States, 63130

New York

Hospital for Special Surgery, New York, New York, United States, 10021

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Skeletally mature patient undergoing Bernese periacetabular osteotomy for symptomatic acetabular dysplasia/hip instability
  • * Pre-Operative MRI at 3T and/or gadolinium MR arthrogram
  • * Age, 16-50 years old
  • * Patient capable of giving informed consent
  • * Prior hip/pelvis surgery of any kind on the surgical side
  • * Prior hip arthroplasty surgery on either side
  • * Radiographic evidence of arthritis (i.e. Tönnis grade =2)
  • * Known connective tissue disorder (e.g. Ehlers-Danlos Syndrome, etc.)
  • * Known neuromuscular disorder (e.g. Cerebral Palsy, Spina bifida, etc.)
  • * Known skeletal dysplasia (e.g. Achondroplasia, Multiple Epiphyseal Dysplasia, etc.)
  • * Cognitive impairment that prevents accurate completion of patient-reported outcome questionnaires.
  • * Patient unable/unwilling to complete all required follow-up visits
  • * Concurrent proximal femoral osteotomy and/or surgical hip dislocation

Ages Eligible for Study

16 Years to 50 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Ottawa Hospital Research Institute,

Geoffrey Wilkin, MD, PRINCIPAL_INVESTIGATOR, The Ottawa Hospital Research Institute

Study Record Dates

2024-12-31