Example: Heart Attack
Clinical Trials on Lipid Metabolism, Inborn Errors
Total 745 results
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NCT02707211Unknown statusConditions: Lipid Metabolism, Inborn Errors
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NCT00092898CompletedConditions: Lipid Metabolism, Inborn Errors; Heart Disease
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NCT00092820CompletedConditions: Lipid Metabolism, Inborn Errors; Heart Disease
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NCT00092807CompletedConditions: Lipid Metabolism, Inborn Errors; Heart Disease
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NCT00004481CompletedConditions: Lipid Metabolism, Inborn Errors; Sitosterolemia
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NCT00092833TerminatedConditions: Hypercholesterolemia, Familial; Lipid Metabolism, Inborn Errors
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NCT03198897Active, not recruitingConditions: Lipoprotein Lipase Deficiency; Inborn Error of Lipid Metabolism; Corneal Arcus
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NCT01782027SuspendedConditions: Cholesterol, HDL; Lipid Metabolism, Inborn Errors; Tangier Disease; LCAT Deficiency; Cholesteryl Ester Transfer Protein (CETP) Deficiency
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NCT00260299TerminatedConditions: Mevalonic Aciduria; Mevalonate Kinase Deficiency; Immune System Diseases; Periodic Fever Syndromes, Hereditary; Lipid Metabolism, Inborn Errors
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NCT01916512Unknown statusConditions: Low CETP Activity; CETP Deficiency; Hyperalphalipoproteinemia; Hyper-LDL-cholesterolemia; High Level of Remnant Cholesterol
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NCT03393130Unknown statusConditions: Cognitive Impairment; Apolipoprotein E, Deficiency or Defect of; Critical Illness; Burns; Young Adult
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NCT03531554CompletedConditions: VLCAD Deficiency; Fatty Acid Oxidation Defects
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NCT01584206CompletedConditions: Sitosterolemia
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NCT02635269Active, not recruitingConditions: Metabolism, Inborn Errors; Lipid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency; Glycogenin-1 Deficiency (Glycogen Storage Disease Type XV); Carnitine Palmitoyl Transferase 2 Deficiency; VLCAD Deficiency; Medium-chain Acyl-CoA Dehydrogenase Deficiency; Multiple Acyl-CoA Dehydrogenase Deficiency; Carnitine Transporter Deficiency; Neutral Lipid Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Glycogen Storage Disease Type V; Muscle Phosphofructokinase Deficiency; Phosphoglucomutase 1 Deficiency; Phosphoglycerate Mutase Deficiency; Phosphoglycerate Kinase Deficiency; Phosphorylase Kinase Deficiency; Beta Enolase Deficiency; Lactate Dehydrogenase Deficiency; Glycogen Synthase Deficiency
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NCT00694109CompletedConditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
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NCT00607373CompletedConditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
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NCT00477594CompletedConditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
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NCT00362180CompletedConditions: Lipid Metabolism, Inborn Errors; Hyperlipidemias; Metabolic Diseases; Hypolipoproteinemia; Hypolipoproteinemias; Hypobetalipoproteinemias; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Congenital Abnormalities; Metabolic Disorder; Hypercholesterolemia; Dyslipidemias; Lipid Metabolism Disorders
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NCT03384420Enrolling by invitationConditions: Mitochondrial Diseases; Pearson Syndrome
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NCT02327364CompletedConditions: Pearson Syndrome
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NCT02104336TerminatedConditions: Pearson Syndrome
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NCT03875105Not yet recruitingConditions: Lipid Storage Disease
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NCT02918032RecruitingConditions: Neutral Lipid Storage Disease
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NCT01527318CompletedConditions: Neutral Lipid Storage Disease
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NCT02830763TerminatedConditions: Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)