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

NCT06444503 — Recruiting, 350 participants, University Hospital, Toulouse

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Creation of a Biological Collection to Study the Pathophysiology and Identify Predictive Factors for the Evolution of Bone, Calcium and Growth Plate Pathologies

RegistryNCT06444503, acronym OSCAR
StatusRecruiting
Study typeObservational
Enrollment350 (Estimated)
SponsorUniversity Hospital, Toulouse (Other)
ConditionsBone Disorder
InterventionsBiological samples, Biological (Other)
Datesstart 2024-09-16, primary completion 2034-09-16 (estimated), completion 2034-09-16 (estimated), first posted 2024-06-05, last updated 2026-06-05
Locations1 site in France

Related Papers Related Patents Related Grants Related Experts
All trials for Bone Disorder All trials of Biological samples All trials of Biological

-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.

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+Arms and interventions

ArmTypeInterventionsDescription
Patients suffering from growth plate or bone pathologyOther: Biological samples; Other: BiologicalAs part of their pathology, patients benefit from clinical monitoring and regular blood and urine tests.
  • Biological samples (Other): Blood and urine will be taken in larger quantity
  • Biological (Other): Surgical residues may be preserved in the event of surgery carried out as part of the treatment.

+Outcome measures

Primary outcomes

  • 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

Secondary outcomes

  • Identification of potential markers of disease progression based on new knowledge. [Day 0 and through study completion, an average of 5 years]

+Eligibility

Sex: All, ages: any to 99 Years

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

+Locations (1)

FacilityCityCountryStatus
University Toulouse HospitalToulouseFranceRecruiting

+Investigators

  • Thomas EDOUARD, MD, Principal investigator, University Hospital, Toulouse