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LCHAD deficiency

Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-3 of 3 results.
Fatty Acid Oxidation Defects and Insulin Sensitivity
Status: Recruiting
Last Changed: Jul 17, 2019
First Received: Aug 07, 2015
Disease(s): Very Long-chain Acyl-CoA Dehydrogenase Deficiency, Trifunctional Protein Deficiency, Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency, Medium-chain Acyl-CoA Dehydrogenase Deficiency, Normal Volunteers, Carnitine Palmitoyltransferase II Deficiency, Myopathic
Intervention(s): Intralipid/Heparin, Glycerol/Saline, Hyperinsulinemic euglycemic clamp
Locations: Oregon Health & Science University, Portland, Oregon, United States
Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy
Status: Recruiting
Last Changed: Sep 01, 2017
First Received: Dec 18, 2015
Disease(s): 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
Intervention(s): Sugar
Locations: Neuromuscular Research Unit, 3342, Copenhagen, Denmark
Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism
Status: Available
Last Changed: Aug 26, 2019
First Received: Oct 28, 2011
Disease(s): Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency, Carnitine Palmitoyltransferase Deficiencies (CPT1, CPT2), Mitochondrial Trifunctional Protein Deficiency, Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency, Glycogen Storage Disorders, Pyruvate Carboxylase Deficiency Disease, ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY of, Barth Syndrome
Intervention(s): triheptanoin
Locations: University of Pittsburgh Division of Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States