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Recruiting Observational

Calcium Isotope Ratios to Assess Calcium Bone Balance in Dialysis Children Receiving Cinacalcet

NCT07007338 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-04-29
Last updated
2026-05-22

Condition(s) studied

Children Over 3 Undergoing Dialysis With Secondary Hyperparathyroidism

Investigational drug(s) / intervention(s)

Supplementary blood samples and urines samples

Supplementary blood samples and urines samples: Supplementary blood and urines samples realised during routine visits

Study summary

Managing bone and mineral disorders associated with chronic kidney disease (CKD-MBD) in children is a complex task. Controlling parathyroid hormone (PTH) levels involves adjusting calcium intake, managing hyperphosphatemia, intensive dialysis, and considering specific therapies like active vitamin D analogues and cinacalcet.

Cinacalcet, authorized in Europe since 2017 for children over 3 undergoing dialysis with secondary hyperparathyroidism (SHPT), has shown efficacy in reducing PTH levels. The 2019 guidelines call for its use with caution particularly to avoid hypocalcemia, in children with severe hyperparathyroidism despite optimized conventional treatments.

In adults, cinacalcet has been found to reduce serum PTH, calcium, and phosphate levels, decrease the risk of vascular calcification, and have a positive effect on bone formation. This suggests that cinacalcet may slow the progression of cardiovascular calcifications.

Additionally, Professor Shroff has introduced a non-invasive method for assessing bone calcium status by analyzing stable calcium isotope ratios in blood. This method would allow to determine whether a treatment such as cinacalcet has a positive influence on bone calcium balance, a key element in the management of CKD-MBD.

Eligibility

Sex
ALL
Min age
3 Years
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: * Children from 3 to 17 years of age * On maintenance dialysis : hemodialysis, hemodiafiltration, peritoneal dialysis * Patient who begin treatment with cinacalcet based on the 2019 European guidelines and at the discretion of the treating physician * With normal QTc interval on electrocardiogram * With total serum calcium \>2.40 mmol/L * With heamoglobin \> 8g/dl * Non - opposition from parents/legal guardians Exclusion Criteria: * Children \< 12 kg * Persons deprived of their liberty by a judicial or administrative decision * Persons under psychiatric care * Persons admitted to a health or social institution for purposes other than research * Persons not affiliated to a social security scheme or beneficiaries of a similar scheme * Persons participating in other interventional research with an exclusion period still in progress at pre-inclusion * Patients who received cinacalcet with 3 months prior inclusion

Primary outcome measure(s)

  • value of isotope ratios of calcium (44/42 Ca) in blood — Baseline / 3 months treatment
    value of 44/42 Ca ratio in patients at baseline and, three months after cinacalcet treatment

Trial sites (7)

FacilityCityRegionStatus
Service de Pédiatrie CHU de Bordeaux Bordeaux France Recruiting
Hôpital Femme Mère Enfant Bron France Recruiting
Service de pédiatrie multidisciplinaire CHU de Montpellier Montpellier France Recruiting
Unité de néphrologie pédiatrique, Hôpital Archet 2, CHU de Nice Nice France Recruiting
Service de Néphrologie pédiatrique Hôpital Necker Enfants Malades Paris France Recruiting
Service de Néphrologie - Transplantation - Hémodialyse pédiatrique Hôpital Robert Debré Paris France Recruiting
Service de pédiatrie 1 CHU Hautepierre Strasbourg France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07007338 on ClinicalTrials.gov ↗ ← All trials in France