Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation (CTX)
Heart Transplantation, Liver Transplantation, Bone Resorption
About this trial
This is an interventional prevention trial for Heart Transplantation focused on measuring Heart Transplantation, Liver Transplantation, Immunosuppression, Bone Density/drug effects, Alendronate, Zoledronic acid, Comparative study, Humans
Eligibility Criteria
Inclusion Criteria: A man or woman, aged 20 to 70, of any race who has had a heart or liver transplant Exclusion Criteria: hyperparathyroidism Paget's disease hyperthyroidism cancer severe kidney disease, intestinal disease active peptic ulcer disease current or past treatment for osteoporosis pregnancy or lactation severe oral/dental disease
Sites / Locations
- Columbia University Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Active Zoledronic Acid & Placebo Alendronate
Placebo Zoledronic Acid & Active Alendronate
Group 1 will receive an infusion of active zoledronic acid 5 mg during the first 4 weeks after transplantation. Placebo alendronate 70 mg once weekly will be initiated at the same time as the first zoledronic acid infusion.
Group 2 will receive an infusion of placebo zoledronic acid during the first 5 weeks after transplantation. Active alendronate 70 mg once weekly will be initiated at the same time as the placebo infusion.