Example: Heart Attack
Clinical Trials on Lipidoses
Total 446 results
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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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NCT04106544RecruitingConditions: Sphingomyelin Lipidosis
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NCT02292654CompletedConditions: Sphingomyelin Lipidosis
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NCT02004704Active, not recruitingConditions: Sphingomyelin Lipidosis
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NCT02004691Active, not recruitingConditions: Sphingomyelin Lipidosis
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NCT03534414Unknown statusConditions: Cardiovascular Risk Factor; Cholesterol; Lipidosis
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NCT02830763TerminatedConditions: Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)
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NCT04373863RecruitingConditions: Cholesterol; Lipidosis; Arterial Hypertension; Blood Glucose, High
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NCT00045812CompletedConditions: Lipoidosis
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NCT04761952Not yet recruitingConditions: Inflammatory Bowel Diseases; Crohn Disease; Polyunsaturated Acid Lipidosis
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NCT00358943RecruitingConditions: Gaucher Disease; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease
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NCT00365131CompletedConditions: Gaucher Disease Type I; Cerebroside Lipidosis Syndrome; Clucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
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NCT00364858CompletedConditions: Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
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NCT00358150CompletedConditions: Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form
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NCT03542370Unknown statusConditions: Cardiovascular Risk Factor; Cardiovascular Diseases; Coronary Heart Disease; Stroke; Diabetes; Blood Pressure; Cholesterol; Lipidosis; Inflammation; Adiposity
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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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NCT02993796RecruitingConditions: Krabbe Disease
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NCT02416661CompletedConditions: Lysosomal Storage Diseases; Gaucher Disease; Sphingolipidoses
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NCT02069106WithdrawnConditions: Mixed Hyperlipoproteinemia
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NCT01974297Unknown statusConditions: Mixed Hyperlipidemia
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NCT00289900CompletedConditions: Mixed Hyperlipidemia
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NCT00134238TerminatedConditions: Mixed Hyperlipidemia
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NCT01306604Active, not recruitingConditions: Niemann-Pick Disease; Niemann-Pick Disease, Type C