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Recruiting Observational

Clinico-biological Collection of Bone, Calcium and Growth Plate Pathologies

NCT06444503 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-09-16
Last updated
2026-06-05

Condition(s) studied

Bone Disorder

Investigational drug(s) / intervention(s)

Biological samplesBiological

Biological samples: Blood and urine will be taken in larger quantity

Biological: Surgical residues may be preserved in the event of surgery carried out as part of the treatment.

Study summary

The aim of this project is to set up a biological and clinical collection of patients with progressive bone, calcium and growth plate pathologies.

This collection will provide a better understanding of the mechanisms involved in growth plate and bone damage in these diseases and identify factors predictive of progression and new therapeutic targets.

Eligibility

Sex
ALL
Min age
—
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria: * Children (from birth) with growth plate or bone pathology * Patients affiliated to or benefiting from a social security scheme * Patients able to receive information about the study and to understand the information form in order to participate in the study. This implies : * mastery of the French language * Not being subject to a restriction of rights by the judicial authorities * Patients or legal representatives having given their consent to participate in the study (expression of non-opposition). Exclusion Criteria: * Patients under legal protection (guardianship, curatorship or safeguard of justice) * Pregnant or breast-feeding women

Primary outcome measure(s)

  • Building a collection of biological samples and clinical-biological data from patients presenting bone, calcium and growth plate pathologies — Day 0 and through study completion, an average of 5 years
    Blood and urine sampling

Trial sites (1)

FacilityCityRegionStatus
University Toulouse Hospital Toulouse 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 NCT06444503 on ClinicalTrials.gov ↗ ← All trials in France