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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01575977
Other study ID # 43600
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 2011
Est. completion date August 2019

Study information

Verified date October 2019
Source University of Utah
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date August 2019
Est. primary completion date August 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility 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 Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Utah

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 1 year post surgery
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