hyperlipoproteinemia type 3 | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
HoFH, the International Clinical Collaborators Registry	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Hypercholesterolemia, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A, familial hypercholesterolemia, hereditary disease, homozygous familial hypercholesterolemia, hyperlipidemia, hyperlipoproteinemia, hyperlipoproteinemia type 3, inborn errors of metabolism, metabolic disease	Recruiting	Not stated	2025-12-18		NCT04815005
Integrating Whole Genome Sequencing and Digital Twins Into the Management of Hypercholesterolemia in Emiratis	Autosomal Recessive Hypercholesterolemia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Hyperlipoproteinemia Type IIa, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, familial hypercholesterolemia, hereditary disease, hyperlipidemia, hyperlipoproteinemia, hyperlipoproteinemia type 3, inborn errors of metabolism, metabolic disease	Recruiting	Not applicable	2025-03-25		NCT06535542
Genetic Testing and Motivational Counseling for FH	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Hypercholesterolemia, Hyperlipoproteinemia Type IIa, Hyperlipoproteinemia Type IIb, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, familial hypercholesterolemia, hereditary disease, hypercholesterolemia, autosomal dominant, 3, hypercholesterolemia, autosomal dominant, type B, hypercholesterolemia, familial, 1, hypercholesterolemia, familial, 4, hyperlipidemia, hyperlipoproteinemia, hyperlipoproteinemia type 3, inborn errors of metabolism, metabolic disease	Active, not recruiting	Not applicable	2024-12-17		NCT04656028