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Stress Analysis of Hip Dysplasia

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ClinicalTrials.gov Identifier: NCT01575977
Recruitment Status : Completed
First Posted : April 12, 2012
Last Update Posted : November 4, 2019
Sponsor:
Information provided by (Responsible Party):
Andrew Anderson, University of Utah

Study Description
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Brief Summary:
The main objective of this study is to predict cartilage contact pressures in the hip after periacetabular osteotomy (PAO).

Condition or disease
Hip Dysplasia

Detailed Description:
PAO was designed as a joint preserving surgical procedure to compensate for a shallow acetabulum by re-orienting the acetabulum into a position that provides better coverage of the femoral head. Although the overall theory that increasing load bearing area (improving coverage of the femoral head) results in reduced joint stress is intuitive, the complex bony surface may not behave in this manner. It is possible that joint stress may increase when the acetabulum is reoriented into a position that increases load bearing area if post-operative joint congruency is worse than pre-operative.
Study Design
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Study Type : Observational
Actual Enrollment : 12 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Stress Analysis of Hip Dysplasia After Corrective Surgery
Study Start Date : February 2011
Actual Primary Completion Date : August 2019
Actual Study Completion Date : August 2019
Groups and Cohorts
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Outcome Measures
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Primary Outcome Measures :
  1. To predict cartilage contact pressures in the hip joint during simulated daily activities before and after periacetabular osteotomy (PAO) for correction of traditional dysplasia/retroversion. [ Time Frame: 1 year post surgery ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
18-40 years old
Criteria

Inclusion Criteria:

  • Patients aged 18-40 years
  • Patients who have undergone periacetabular osteotomy by Dr. Peters for treatment of hip dysplasia.
  • Patients who have previously participated in IRB #10983 "Comparative Stress Analysis of Hip Dysplasia".

Exclusion Criteria:

  • Persons with a history of allergies to lidocaine or seafood.
  • Children under the age of 18.
  • Persons incarcerated, on trial, or parole.
  • Women who are pregnant.
  • Subjects who do not have high quality pre-operative images available or have not been surgically treated by periacetabular osteotomy.
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01575977


Sponsors and Collaborators
University of Utah
Investigators
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Principal Investigator: Andrew Anderson Orthopedic Surgery Operations
More Information
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Responsible Party: Andrew Anderson, Associate Professor, University of Utah
ClinicalTrials.gov Identifier: NCT01575977    
Other Study ID Numbers: 43600
First Posted: April 12, 2012    Key Record Dates
Last Update Posted: November 4, 2019
Last Verified: October 2019
Additional relevant MeSH terms:
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Hip Dislocation
Hip Dislocation, Congenital
Joint Dislocations
Joint Diseases
Musculoskeletal Diseases
 Wounds and Injuries
Hip Injuries
Musculoskeletal Abnormalities
Congenital Abnormalities