Osteoarthritis Clinical Trial
Official title:
Clinical Evaluation of Taperloc Total Hip System With Two Different Stem Lengths
This evaluation is conducted to evaluate the safety and performance of two different stem lengths of the Taperloc Total Hip System. Per implant bone loss and migration of the stem are compared between the two groups with Dual-energy X-ray absorptiometry (DEXA) and radiostereomektric analysis
Consecutive patients between 50 - 70 years diagnosed with primary osteoarthritis of the hip
and eligible for total hip arthroplasty will be asked to participate in the study.
Periprosthetic bone loss, migration of the components and clinical scores will be recorded
prospectively at 3,6,12 and 24 months.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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