Arthroplasty Clinical Trial
The purpose of this study was to develop a radiological method to measure stem anteversion and to determine its validity and reliability.
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Investigators recruited 40 consecutive patients who underwent THR between October 2015 and December 2015 Exclusion Criteria: - patients who could not extend the hip because of a residual flexion contracture. - who had a flexion contracture of the knee or who could not flex the hip to 90° even after THR were excluded because participants could not adopt the posture required for the particular radiographs and CT scans. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul national University Bundang Hospital | Seongnam-Si | Gyeounggi-do |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Bundang Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | stem anteversion of the hip radiograph(decubitus lateral view) | postoperative 4days | Yes | |
Primary | stem anteversion of the CT scan | postoperative 4days | Yes | |
Secondary | The correlation between stem anteversion of the decubitus lateral view and stem version of the CT scan | to determine ICC(intraclass coefficient, correlation coefficient) | postoperative 4days | Yes |
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