Denosumab
DrugDenosumab will be administered at postoperative months 1, 7, and 13
Other names: Prolia
NCT Number: NCT04087096
Bariatric surgery leads to bone loss and increases fracture risk. This study evaluates whether denosumab can prevent the high-turnover bone loss that occurs after Roux-en-Y Gastric Bypass (RYGB) and sleeve gastrectomy (SG) surgery.
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Notify Me25 year and older
All sexes
Interventional
Phase 4
University of California, San Francisco, San Francisco, California, United States
Bariatric surgery is a highly effective weight loss treatment, but one of the unintended side effects of these procedures is high-turnover bone loss and metabolic bone disease. Denosumab is a monoclonal antibody to RANKL that acts as a potent inhibitor of bone resorption. The investigators are conducting a randomized placebo-controlled trial to evaluate the ability of denosumab to prevent bone loss after RYGB or SG surgery in older adults. At the conclusion of the study, all participants will be given zoledronic acid.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Denosumab will be administered at postoperative months 1, 7, and 13
Other names: Prolia
Placebo will be administered at postoperative months 1, 7, and 13
Zoledronic Acid 5mg will be administered intravenously at postoperative month 19
Other names: Reclast
Time frame: Pre-operative baseline to post-operative month 19
Massachusetts General Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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