At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 120 enrolled
Drug / intervention
Stemless femoral component +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Periprosthetic Bone Mineral Changes Around Stemless and Stemmed Cementless Femoral Components
In Brief
A Phase 4 clinical trial evaluating Stemless femoral component and IPS, Depuy cementless femoral stem for Osteoarthritis of Hip. Completed, enrolled 120 participants across 1 site.
Detailed Summary
The purpose of this study is to determine if there is a difference in stress shielding and bone resorption of the proximal femur in two anatomical stem total hip designs.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOsteoarthritis of Hip
CountriesSouth Korea
Collaborators--
Timeline
Phase 4CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJul 2006
Primary CompletionJul 2007
Study CompletionJul 2009
First PostedAug 2009
TodayJul 2026
First PostedAug 13, 2009
Enrollment StartJul 1, 2006
Primary CompletionJul 1, 2007
Study CompletionJul 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 16.9 years ago
Interventions
Stemless femoral componentdevice
Total hip femoral component anatomically designed for a proximal fit without a stem
IPS, Depuy cementless femoral stemdevice
Anatomical proximal fitted cementless stemmed femoral component