Prevention of Periprosthetic Bone Loss After Total Hip Replacement by Annual Bisphosphonate Therapy

This study is a prospective, randomized, open-label clinical trial. The study will be performed in patients after obtaining informed consent. Group assignment is by drawing a sealed envelops based on random table. (1) Group 1: Experimental group 30 cases, Aclasta® (Zoledronic acid 5mg/100ml) is given intravenously on the 4th postoperative day and one year after the total hip replacement, (2) Group 2: Control group, 30 cases, no bisphosphonate is given to the patients. Only the unilateral coxarthrosis will be recruited for the study. Patients will be analyzed with (1) DXA study (2) Clinical assessment (Harris hip score and SF-12) (3) X-ray (4) serum marker of bone turnover. Patients will be scheduled for specified examinations preoperatively, postoperatively 6 weeks, 3 months, 6 months, 12 months, and 24 months.

Inclusion criteria

• Male or female,between 35 and 85 years of age
• Indicated for Total hip replacement for various hip diseases
• Has preoperative DXA study within 3 months before the total hip replacement procedure or willing to receive preoperative DXA study as a baseline comparison
• Signed written informed consent
• Standard transgluteal approach for total hip replacement using Zimmer Triology Cup and Versys Fiber Metal Taper Stem with metal to highly cross-linked polyethylene bearing surface

Exclusion criteria

• Any prior use of intravenous bisphosphonate within the last 2 years
• Uncontrolled seizure disorders associated with falls
• A history of invasive malignancy of any organ system, treated or untreated, within the past five years; excluding, basal cell or squamous cell carcinoma of the skin, colonic polyps with non-invasive malignancy which have been removed
• Carcinoma in situ of the uterine cervix
• History of osteogenesis imperfecta, multiple myeloma, or Paget's disease
• Active primary hyperparathyroidism
• History of iritis or uveitis
• Self-reported history of diabetic nephropathy or retinopathy
• AST or ALT more than twice the upper limit of normal
• Alkaline phosphatase more than twice the upper limit of normal
• Serum calcium 2.75 mmol/L (11.0 mg/dL)
• Baseline renal insufficiency (calculated creatinine clearance 35 ml/min)
• History of hypersensitivity to bisphosphonates
• Use of any investigational drug(s) and/or devices within 30 days prior to randomization
• Any medical or psychiatric condition which, in the Investigator's opinion, would preclude the participant from adhering to the Protocol or completing the trial per protocol
• Use of hip protectors
• With implant or prosthesis on the contralateral hip joint