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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
FARD (RaDiCo Cohort) (RaDiCo-FARD)Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Conjunctival Diseases, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Keratoderma, Palmoplantar, Neoplasms by Histologic Type, Neoplasms, Nerve Tissue, Nutritional and Metabolic Diseases, Pemphigoid, Benign Mucous Membrane, Skin Abnormalities, Skin and Connective Tissue Diseases, albinism, autoimmune disease, ectodermal dysplasia syndrome, eye disorder, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, immune system disorder, inborn disorder of amino acid metabolism, inborn errors of metabolism, incontinentia pigmenti, inherited epidermolysis bullosa, inherited neurodegenerative disorder, keratosis, metabolic disease, mucous membrane pemphigoid, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neurofibroma, neurofibromatosis, neurofibromatosis type 1, neuromuscular disease, pemphigus, peripheral nervous system disorder, skin disorder, skin pigmentation disorder, vesiculobullous skin diseaseRecruitingNot stated2026-02-12NCT05954416

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Research sitesCityCountryLinked trials
Hôpital AvicenneBobignyFrance13
Hôpital Charles NicolleRouenFrance9
Hôpital de La TimoneMarseilleFrance17
Hôpital des Enfants - Groupe Hospitalier PellegrinBordeauxFrance2
Hôpital DupuytrenLimogesFrance3
Hôpital François MitterrandDijonFrance4
Hôpital Henri-MondorCréteilFrance3
Hôpital l'ArchetNiceFrance3
Hôpital LarreyToulouseFrance2
Hôpital Necker-Enfants maladesParisFrance8
Hôpital Robert-DebréReimsFrance1
Hôpital Saint-EloiMontpellierFrance4
Hôpital Saint-LouisParisFrance16
Hôpital TrousseauToursFrance5