- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01657357
Routine Follow up After Total Hip Arthroplasty Prior Periacetabular Osteotomy
January 30, 2013 updated by: University of Aarhus
Routine Follow up After THA in PAO Patient
Follow up study of patients, who despite periacetabular osteotomy, need a total hip arthroplasty, to see outcome.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Aarhus, Denmark, 8000
- Orthopaedic department, Aarhus Universityhospital
-
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients, who despite a joint preserving procedure(periacetabular osteotomy PAO) ended up with a total hip arthroplasty (THA).
Description
Inclusion Criteria:
- PAO and THA
Exclusion Criteria:
- time since THA less than 4 yrs
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
PAO, osteoarhritis, THA
|
questionnaires
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Does previous PAO compromise the function of a secondary THA
Time Frame: Up to 10 years after THA surgery
|
To describe the radiographic status (ex.
cup positioning, calcifications, signs of loosing etc) of the THA, the physical function of the THA ( Harris Hip Score), and pt reported outcome measurements (SF36 and WOMAC).
|
Up to 10 years after THA surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Kjeld Soballe, Prof. D.Msc, Orthopedic Research Unit, Aarhus University Hospital
- Principal Investigator: Charlotte Hartig-Andreasen, MD, Orthopedic Research Unit, Aarhus University Hospital
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
January 1, 2012
Primary Completion (Actual)
August 1, 2012
Study Completion (Actual)
October 1, 2012
Study Registration Dates
First Submitted
March 13, 2012
First Submitted That Met QC Criteria
August 1, 2012
First Posted (Estimate)
August 6, 2012
Study Record Updates
Last Update Posted (Estimate)
January 31, 2013
Last Update Submitted That Met QC Criteria
January 30, 2013
Last Verified
January 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- THA after PAO
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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