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Very long chain acyl-CoA dehydrogenase deficiency

VCLAD deficiencyACADVL
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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: Apr 09, 2020
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
Expanded Access to Triheptanoin
Status: Available
Last Changed: May 20, 2020
First Received: Dec 12, 2018
Disease(s): Long-chain Fatty Acid Oxidation Disorders (LC-FAOD), Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)
Intervention(s): Triheptanoin
Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism
Status: Available
Last Changed: Dec 16, 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