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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
IDMet (RaDiCo Cohort) (RaDiCo-IDMet)Abnormalities, Multiple, Angelman syndrome, Beckwith-Wiedemann syndrome, Bone Diseases, Metabolic, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dwarfism, Imprinting Disorders, Musculoskeletal Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Prader-Willi syndrome, Silver-Russell syndrome, Temple syndrome, bone disorder, calcium metabolic disease, central nervous system disorder, chromosomal disorder, endocrine system disorder, gonadal disorder, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, intellectual disability, metabolic disease, movement disorder, multiple congenital anomalies due to 14q32.2 maternally expressed gene defect, musculoskeletal system disorder, nervous system disorder, nutritional disorder, obesity disorder, overnutrition, paternal uniparental disomy of chromosome 14, precocious puberty, pseudohypoparathyroidism, transient neonatal diabetes mellitusRecruitingNot stated2026-02-12NCT05945576

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Research sitesCityCountryLinked trials
CHU d'AngersAngersFrance27
Hôpital Armand-TrousseauParisFrance3
Hôpital BicêtreLe Kremlin-BicêtreFrance15
Hôpital BraboisNancyFrance3
Hôpital BretonneauToursFrance4
Hôpital CivilStrasbourgFrance2
Hôpital de la mère et de l'enfantLimogesFrance1
Hôpital de la Pitié-SalpêtrièreParisFrance4
Hôpital de La TimoneMarseilleFrance17
Hôpital des EnfantsToulouseFrance3
Hôpital enfant-adolescentNantesFrance1
Hôpital Femme Mère EnfantLyonFrance3
Hôpital Gabriel MontpiedClermont-FerrandFrance7
Hôpital Jean MinjozBesançonFrance4
Hôpital Jeanne de FlandreLilleFrance3
Hôpital Necker Enfants MaladesParisFrance8
Hôpital Robert DebréParisFrance11
Hôpital SudRennesFrance1