- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02552173
The Relationship Between Operative and Radiologic Stem Version
March 28, 2016 updated by: Kyung-Hoi Koo, Seoul National University Bundang Hospital
The Relationship Between Operative and Radiologic Stem Version : Which Factors Influence Resultant Stem Version in Primary Total Hip Arthroplasty
Investigators prospectively evaluate the accuracy of intraoperative stem anteversion in 40consecutive total hip arthroplasties.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In all hips, investigators measure femoral stem anteversion postoperatively with three-dimensional computed tomography reconstruction of the femur, using both the distal femoral epicondyles and the posterior femoral condyles to determine the femoral diaphyseal plane.
And investigators compare the surgeon's estimate of intraoperative stem version and stem version of CT scan.
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
-
-
Gyeounggi-do
-
Seongnam-Si, Gyeounggi-do, Korea, Republic of, 463-707
- Seoul National University Bundang Hospital
-
-
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
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Between October 2015 and December 2015, 40 consecutive patients who underwent primary cementless total hip arthroplasty agreed to undergo a postoperative computed tomography scan.
Description
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.
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 |
|---|---|
|
stem anteversion
intraoperative surgeon's estimation and postopertive CT sacn were taken to measure stem anteversion
|
intraopertive surgeon's estimation and postoperative CT scan
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Intraopertive surgeon's estimation and postoperative CT scan were taken to measure stem anteversion
Time Frame: postoperative 4days
|
postoperative 4days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The correlation between stem anteversion of intraopertive surgeon's estimation and stem version postoperative CT scan
Time Frame: postoperative 4days
|
to determine ICC(intraclass coefficient, correlation coefficient)
|
postoperative 4days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Kyung-Hoi Koo, professor, Director, Head of Orthopaedics, Seoul National university Bundang 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
October 1, 2015
Primary Completion (Actual)
March 1, 2016
Study Completion (Actual)
March 1, 2016
Study Registration Dates
First Submitted
September 15, 2015
First Submitted That Met QC Criteria
September 15, 2015
First Posted (Estimate)
September 17, 2015
Study Record Updates
Last Update Posted (Estimate)
March 29, 2016
Last Update Submitted That Met QC Criteria
March 28, 2016
Last Verified
March 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- Ante-002
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.
Clinical Trials on Arthroplasty Total Hip Replacement
-
The Royal Bournemouth HospitalCompletedArthroplasty, Replacement, Hip | Hip Replacement, TotalUnited Kingdom
-
Ortho Development CorporationOregon Health and Science UniversityEnrolling by invitationTotal Hip Replacement | Total Hip ArthroplastyUnited States
-
National Taiwan University HospitalUnknownTotal Hip Replacement | Total Hip ArthroplastyTaiwan
-
Solventum US LLCRecruitingArthroplasty Replacement, Knee | Arthroplasty Total Hip ReplacementUnited States
-
Musgrave Park HospitalBelfast Health and Social Care Trust; Queen's University, Belfast; Belfast Arthroplasty...CompletedTotal Hip Replacement | Total Hip Arthroplasty | THA | THRUnited Kingdom
-
ElsanNot yet recruitingPrimary Total Hip Arthroplasty | Primary Total Hip ReplacementFrance
-
Desert Orthopedic Center Medical Research FoundationBaxter Healthcare CorporationUnknownTotal Knee Arthroplasty | Arthroplasty, Replacement, HipUnited States
-
Ospedale Edoardo BassiniCompletedRegional Anesthesia | Regional Anesthesia Block | Total Hip Replacement Surgery | Total Hip Arthroplasty \(THA\)Italy
-
Ottawa Hospital Research InstituteUnknownArthroplasty, Replacement, Hip | Hip Replacement, TotalCanada
-
Hospital for Special Surgery, New YorkRecruitingPain | Pain Management | Randomized Controlled Trial | Total Hip Replacement | Multimodal Analgesia | Randomized Controlled Study | Total Hip Replacements | Total Hip Replacement Surgery | Total Hip Arthroplasty (THA) | Opioid Cessation | Randomized Controlled Trials | Total Hip Replacement Arthroplasty | Opioid... and other conditionsUnited States
Clinical Trials on The Relationship Between Operative and Radiologic Stem Version
-
Sanliurfa Education and Research HospitalCompletedUmbilical Cord Coiling Index and Fetal Cardiac FunctionsTurkey (Türkiye)
-
Saglik Bilimleri UniversitesiNot yet recruiting
-
Selcuk UniversityCompletedNystagmus Vestibular | Positional Vertigo | Reflexes, Vestibo-OcularTurkey
-
National Heart, Lung, and Blood Institute (NHLBI)CompletedHypertension | Healthy | HypercholesterolemiaUnited States
-
Tokat Gaziosmanpasa UniversityCompletedPain | Temporomandibular Disorder | Spine | Discomfort | Geriatric IndividualsTurkey
-
Hospices Civils de LyonRecruiting
-
The Affiliated Hospital of Hangzhou Normal UniversityNot yet recruitingHypertensive Emergency
-
Rennes University HospitalCompletedSupraventricular ArrhythmiasFrance
-
Yuzuncu Yıl UniversityCompleted