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Completed

NCT Number: NCT04087096

Denosumab to Prevent High-Turnover Bone Loss After Bariatric Surgery

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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Key information

Age range

25 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of California, San Francisco, San Francisco, California, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Postmenopausal women who are planning RYGB or SG surgery
  • Men aged ≥ 50 years who are planning RYGB or SG surgery

Exclusion criteria

  • Prior bariatric surgery
  • Weight = 400 lbs (due to limitations of bone imaging equipment)
  • Renal disease
  • Hypercalcemia or hypocalcemia
  • Hypomagnesemia
  • Serum 25-OH vitamin D (25OHD) < 20 ng/mL
  • Hyperparathyroidism
  • Liver disease (AST or ALT > 2 x upper normal limit)
  • HCT < 32%
  • History of malignancy (except basal cell carcinoma) in the past 1 year
  • Significant cardiopulmonary disease
  • Major psychiatric disease
  • History of celiac disease or inflammatory bowel disease
  • Excessive alcohol or substance abuse
  • Paget's disease, primary hyperparathyroidism, or any other known congenital or acquired bone disease other than osteoporosis
  • Current hyperthyroidism or use of levothyroxine with TSH < 0.1 uIU/mL
  • Current use of loop diuretics
  • Current use or use in the past 12 months of oral bisphosphonates or DMAB
  • Current use or use within the past 3 months of SERMs or calcitonin
  • Current use or use within the past 3 months of estrogen
  • Use of testosterone therapy if dose has changed within the last 3 months, or if dose change or discontinuation is planned in the upcoming 18 months
  • Any current or previous use of teriparatide, strontium, or any parenteral bisphosphonate
  • Use of oral or parenteral glucocorticoids for more than 14 days within the past 6 months
  • Extensive dental work involving extraction or dental implant within the past 2 months or planned in the upcoming 18 months
  • DXA BMD T-score of < -3.0 at PA spine, total hip, or femoral neck
  • Current use of anti-VEGF drug

Treatment and study plan

Denosumab

Drug

Denosumab will be administered at postoperative months 1, 7, and 13

Other names: Prolia

Placebo

Drug

Placebo will be administered at postoperative months 1, 7, and 13

Zoledronic acid

Drug

Zoledronic Acid 5mg will be administered intravenously at postoperative month 19

Other names: Reclast

Primary outcomes

  1. Percentage Change in Total Hip Bone Mineral Density

    Time frame: Pre-operative baseline to post-operative month 19

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • San Francisco VA Health Care System
  • University of California, San Francisco

Registry information

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Sep 12, 2019
Registry last updated
Oct 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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