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Study Evaluating Denosumab on Vascular and Bone Metabolism in Osteoporotic Chronic Kidney Disease (HDENOBS)

Not yet recruiting
Conditions
Chronic Kidney Disease 5D
Osteoporosis
Interventions
Procedure: MDCT (multidetector computed tomography)
Procedure: Dual-energy X-ray absorptiometry
Registration Number
NCT05234047
Lead Sponsor
University Hospital, Montpellier
Brief Summary

Aim of this study is to evaluate in a population of osteoporotic chronic kidney disease patients the effect of denosumab:

* on coronary artery calcification scores evolution after 24 months of followup

* on abdominal aorta calcification scores evolution after 24 months of followup

* on bone mineral density (femoral T-score) at 24 months

* on bone mineral density evolution (femoral T-score) after 24 months of follow-up

* on bone mineral density evolution (lumbar T-score) after 24 months of follow-up

* on parameters of bone remodelling after 24 months of follow-up

* on cardiovascular morbidity (cardiovascular events) and mortality after 24 months of follow-up

* the tolerance after 24 months of follow-up

Detailed Description

Aim of this study is to evaluate in a population of osteoporotic chronic kidney disease patients the effect of denosumab:

* on coronary calcification scores evolution (by multidetector computed tomography) after 24 months of follow-up

* on abdominal aorta calcification scores evolution (by plain abdominal Xray) after 24 months of follow-up

* on bone mineral density (femoral T-score) (by bone densitometry) at 24 months

* on bone mineral density evolution (femoral T-score) (by bone densitometry) after 24 months of follow-up

* on bone mineral density evolution (lumbar T-score) (by bone densitometry) after 24 months of follow-up

* on parameters of bone remodelling after 24 months of follow-up

* on cardiovascular morbidity (cardiovascular events) and mortality after 24 months of follow-up

* the tolerance after 24 months of follow-up

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
21
Inclusion Criteria
  • Chronic kidney disease stage 5D patient, hemodialyzed with extracorporeal treatment for at least 3 months
  • Osteoporosis
Exclusion Criteria
  • Pregnancy or breastfeeeding female
  • Current corticoid treatment
  • PTH and Calcium outside the KDIGO guidelines
  • Adynamic bone disease suspicion
  • Cancer or myeloma
  • Serious hepatic cytolysis
  • Serious dental troubles
  • Positive HIV serology
  • Hypersensibility to active substance or one of excipients of denosumab

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
CKD-5D patients receiving denosumabDual-energy X-ray absorptiometry-
CKD-5D patients receiving denosumabMDCT (multidetector computed tomography)-
Primary Outcome Measures
NameTimeMethod
Relative variation of coronary calcification scores after 24 months of follow-up24 months after inclusion
Secondary Outcome Measures
NameTimeMethod
Relative variation of abdominal aorta calcification scores after 24 months of follow-up24 months after inclusion
Variation of phosphorus at 6, 12, 18 et 24 months of follow-up6, 12, 18 and 24 months after inclusion
Relative variation of femoral bone mineral density after 24 months of follow-up (T-score evaluated by osteodensitometry)24 months after inclusion
Relative variation of whole body bone mineral density after 24 months of follow-up (T-score evaluated by osteodensitometry)24 months after inclusion
Variation of calcium at 6, 12, 18 and 24 months of follow-up6, 12, 18 and 24 months after inclusion]
Variation of inflammation at 6, 12, 18 et 24 months of follow-up6, 12, 18 and 24 months after inclusion
Relative variation of radius bone mineral density after 24 months of follow-up (T-score evaluated by osteodensitometry)24 months after inclusion
Morbi-mortality at 24 months of follow-up24 months after inclusion]
Relative variation of lumbar bone mineral density after 24 months of follow-up (T-score evaluated by osteodensitometry)24 months after inclusion
Variation of bone remodeling at 6, 12, 18 et 24 months of follow-up6, 12, 18 and 24 months after inclusion
Adverse events occuring during the entire study24 months after inclusion]
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