The purpose of this study is to compare the performance of 4 designs of the DePuy Ultima LX hip stem in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the 4 designs of the DePuy Ultima LX hip stem and will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
164
A collared non-polished/blasted finished cementless femoral component for use in total hip replacement.
A collared polished finished cementless femoral component for use in total hip replacement.
A collarless non-polished/blasted finished cementless femoral component for use in total hip replacement.
A collarless polished finished cementless femoral component for use in total hip replacement.
Epsom General Hospital
Surrey, United Kingdom
Stem movement measured radiographically at 2 years
Stem movement was measured radiographically by comparing baseline stem position with the stem position 2 years after surgery. If migration was observed to be 5 or more mm, it was considered clinically significant migration.
Time frame: 2yrs post-surgery
Comparisons of Visual Analog Pain (VAS), 36-Item Short Form Health Survey (SF-36), Satisfaction, Limb Length and stem movement measured radiographically at 5 years.
The following outcome measures were used; VAS Pain score, SF36 Patient reported outcome, Satisfaction, Limb Length physical examination, and stem movement measured radiographically.
Time frame: 5yrs post-surgery
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