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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Application of FreeStyle Libre 2 for Evaluating Glycemic Variability Characteristics in Patients With Extreme Glucose Metabolism PhenotypesNutritional and Metabolic Diseases, glucose metabolism disease, hyperinsulinism, metabolic disease, monogenic diabetesNot yet recruitingNot stated2026-06-02NCT07564518
Glucokinase Activator in Monogenic DiabetesNutritional and Metabolic Diseases, diabetes mellitus, endocrine system disorder, glucose metabolism disease, metabolic disease, monogenic diabetesRecruitingPhase 22026-04-30NCT06976658
China Monogenic Diabetes RegistryNutritional and Metabolic Diseases, diabetes mellitus, endocrine system disorder, glucose metabolism disease, maturity-onset diabetes of the young, metabolic disease, monogenic diabetes, type 2 diabetes mellitusRecruitingNot stated2026-03-25NCT07492004
Understanding Beta Cell Disorders Through the Study of Rare Genotypes (ENDURE)Nutritional and Metabolic Diseases, diabetes mellitus, endocrine system disorder, glucose metabolism disease, hyperinsulinism, metabolic disease, monogenic diabetesRecruitingNot stated2026-01-16NCT06478121
Screening and Molecular Diagnosis-based Individualized Precision Management of Monogenic Diabetesmonogenic diabetesRecruitingNot applicable2024-12-24NCT06746610
Monogenic Diabetes Misdiagnosed as Type 1Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Neurologic Manifestations, Nutritional and Metabolic Diseases, Sensation Disorders, Urogenital Diseases, Wolcott-Rallison syndrome, Wolfram syndrome, autoimmune disease, blindness (disorder), cranial nerve neuropathy, diabetes insipidus, diabetes mellitus, endocrine system disorder, eye disorder, glucose metabolism disease, hearing disorder, hearing loss disorder, hereditary disease, hereditary optic atrophy, immune system disorder, inherited neurodegenerative disorder, kidney disorder, maternally-inherited diabetes and deafness, metabolic disease, monogenic diabetes, nervous system disorder, neurodegenerative disease, optic atrophy, optic nerve disorder, otorhinolaryngologic disease, pituitary gland disorder, type 1 diabetes mellitus, urinary system disorder, vision disorderRecruitingNot stated2024-12-10NCT03988764