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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

350 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-09-16

Study Completion Date

2034-09-16

Brief Summary

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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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Detailed Description

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Conditions

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Bone Disorder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients suffering from growth plate or bone pathology

As part of their pathology, patients benefit from clinical monitoring and regular blood and urine tests.

Biological samples

Intervention Type OTHER

Blood and urine will be taken in larger quantity

Biological

Intervention Type OTHER

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

Interventions

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Biological samples

Blood and urine will be taken in larger quantity

Intervention Type OTHER

Biological

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

Intervention Type OTHER

Eligibility Criteria

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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).