NCT06444503
Not Yet Recruiting
N/A
Creation of a Biological Collection to Study the Pathophysiology and Identify Predictive Factors for the Evolution of Bone, Calcium and Growth Plate Pathologies.
ConditionsBone Disorder
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Bone Disorder
- Sponsor
- University Hospital, Toulouse
- Enrollment
- 350
- Locations
- 1
- Primary Endpoint
- Building a collection of biological samples and clinical-biological data from patients presenting bone, calcium and growth plate pathologies
- Status
- Not Yet Recruiting
- Last Updated
- last year
Overview
Brief 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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Building a collection of biological samples and clinical-biological data from patients presenting bone, calcium and growth plate pathologies
Time Frame: 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)
Study Sites (1)
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