- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01575977
Stress Analysis of Hip Dysplasia
October 31, 2019 updated by: Andrew Anderson, University of Utah
Stress Analysis of Hip Dysplasia After Corrective Surgery
The main objective of this study is to predict cartilage contact pressures in the hip after periacetabular osteotomy (PAO).
Study Overview
Status
Completed
Conditions
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 Type
Observational
Enrollment (Actual)
12
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.
Eligibility Criteria
Ages Eligible for Study
14 years to 36 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
18-40 years old
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
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
|
1 year post surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2011
Primary Completion (Actual)
August 1, 2019
Study Completion (Actual)
August 1, 2019
Study Registration Dates
First Submitted
March 6, 2012
First Submitted That Met QC Criteria
April 11, 2012
First Posted (Estimate)
April 12, 2012
Study Record Updates
Last Update Posted (Actual)
November 4, 2019
Last Update Submitted That Met QC Criteria
October 31, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 43600
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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