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NCT05655013
Treatment With Zoledronate Subsequent to Denosumab in Osteoporosis 2
Conditions: Osteoporosis, Postmenopausal
Sex: Female
Ages: 40 Years – 100 Years
Phase: PHASE4
Enrollment: 200
Sponsor: Aarhus University Hospital
Summary
The aims of ZOLARMAB2 are fourfold.
First, the investigators want to investigate if multiple infusions of zoledronate can prevent the rebound activation of bone turnover and the subsequent bone loss in patients previously treated with denosumab and if there is difference between infusing zoledronate at fixed time-points after the last injection of denosumab or when bone turnover is increased.Second, the investigators want to investigate if bone loss will resume after controlling the rebound activation of bone turnover during the first year after denosumab discontinuation and if this can be prevented by yearly infusions of zoledronate.Third, the investigators want to investigate the underlying pathophysiological mechanisms by investigating biochemical markers, osteoclast and osteoblast activation signals in the bone and bone marrow, and the pool of preosteoclasts/mature osteoclasts before and after treatment with zoledronate.Fourth, the investigators want to investigate the effect of denosumab discontinuation on muscle mass and muscle strength and on insulin sensitivity.
Eligibility Criteria
Inclusion Criteria:Postmenopausal women (postmenopausal for at least two years)Age ≥ 40 yearsTreatment for at least two years with denosumabLast denosumab injection less than five months agoAt least 2 lumbar vertebrae that can be evaluated by DXAExclusion Criteria:Low-energy vertebral fracture at any timeLow-energy hip fracture within the last 12 monthsBMD T-score < -2.0 (lumbar spine, total hip or femoral neck)Bisphosphonate treatment for more than three years prior to denosumab treatmentDiabetes MellitusOngoing treatment with systemic glucocorticoidsMetabolic bone disease (for example osteogenesis imperfecta, Paget's disease of bone)Hormone replacement therapyActive cancer within the last 5 years with the exception of basal cell skin cancerEstimated glomerular filtration rate (eGFR) ≤ 35 mL/minContraindications for zoledronate according to the SPCUnable to read and understand Danish
Source: ClinicalTrials.gov (NCT05655013). StuddyBuddy aggregates publicly available trial information.