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IDMet (RaDiCo Cohort) (RaDiCo-IDMet)

Recruitingn/aAges any - anyAllInstitut National de la Santé Et de la Recherche …
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In plain words

What the trial is, and whether it could suit you

The goal of this observational study is to describe the natural history of imprinting disorders (IDs) according to their metabolic profile in all patients (adults and children) affected with an ID regardless of the severity of the disease, with a molecular characterization, with a signed informed consent for all subjects, followed in one partner's center. The main questions it aims to answer are: * Can we identify common metabolic profiles for all imprinted diseases? * Which imprinting disorders have an impact on the metabolic profiles of IDs? * Which are the metabolic risks associated to IDs? * Can we use the metabolic profiles for the clinical classification and prognosis of IDs? * Are there common therapeutic approaches for all IDs?

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Patients (adults and children) affected with an ID regardless of the severity of the disease * A confirmed diagnosis of ID (based on molecular diagnosis) * A signed informed consent for adults or signed informed consent of parents/guardians of minors/ protected adult. Non-Inclusion Criteria: There are no non-inclusion criteria.
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What it tests

  • Not listed
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Where

20 sites
CHU d'Angers
Angers, France
Hôpital Jean Minjoz
Besançon, France
Hôpital Gabriel Montpied
Clermont-Ferrand, France
Hôpital Bicêtre
Le Kremlin-Bicêtre, France
Hôpital Jeanne de Flandre
Lille, France
Hôpital de la mère et de l'enfant
Limoges, France
Hôpital Femme Mère Enfant
Lyon, France
Hôpital de la Timone
Marseille, France

…and 12 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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