NCT01575977

Brief Summary

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

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2011

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2011

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

March 6, 2012

Completed
1 month until next milestone

First Posted

Study publicly available on registry

April 12, 2012

Completed
7.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2019

Completed
Last Updated

November 4, 2019

Status Verified

October 1, 2019

Enrollment Period

8.5 years

First QC Date

March 6, 2012

Last Update Submit

October 31, 2019

Conditions

Outcome Measures

Primary Outcomes (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.

    1 year post surgery

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

18-40 years old

You may qualify if:

  • 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".

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hip Dislocation

Condition Hierarchy (Ancestors)

Joint DislocationsJoint DiseasesMusculoskeletal DiseasesWounds and InjuriesHip Injuries

Study Officials

  • Andrew Anderson

    Orthopedic Surgery Operations

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

March 6, 2012

First Posted

April 12, 2012

Study Start

February 1, 2011

Primary Completion

August 1, 2019

Study Completion

August 1, 2019

Last Updated

November 4, 2019

Record last verified: 2019-10