2 completed, 2 unknown, 1 recruiting. 5 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 5 | Completed 2, Unknown 2, Recruiting 1 |
Follow Medium chain acyl CoA dehydrogenase deficiency: new trials by email Literature Review of Medium chain acyl CoA dehydrogenase deficiency trials Research Report on Medium chain acyl CoA dehydrogenase deficiency
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| High Intensity Exercise in Children With MCADD Cardiopulmonary exercise test (CPET), High-intensity circuit training - Medium Chain Acyl CoA Dehydrogenase Deficiency | Not applicable | Completed | University Hospital, Ghent | 8 | 2025-01-20 | 2026-03-23 |
| Metabolic Effects of Medium-Chain Fatty Acids in Patients With Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Healthy Individuals Medium-Chain Fatty Acid (MCFA), Long-Chain Fatty Acid (LCFA) - Medium-chain Acyl-CoA Dehydrogenase Deficiency | Not applicable | Recruiting | University of Copenhagen | 30 | 2024-10-18 | 2026-08-14 |
| Fasting Tolerance in MCADD-infants Fasting test - Mcad Deficiency | Not applicable | Unknown | University Medical Center Groningen | 20 | 2019-05-15 | 2019-05-14 |
| Fatty Acid Oxidation Defects and Insulin Sensitivity Intralipid/Heparin, Glycerol/Saline, Hyperinsulinemic euglycemic clamp - Very Long-chain Acyl-CoA Dehydrogenase Deficiency, Trifunctional Protein Deficiency | Not applicable | Completed | Oregon Health and Science University | 41 | 2016-02-01 | 2024-01-30 |
| Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy Sugar - Metabolism, Inborn Errors, Lipid Metabolism, Inborn Errors | Not applicable | Unknown | Copenhagen University Hospital, Rigshospitalet | 60 | 2016-01-01 | 2019-10-16 |
Trifunctional Protein Deficiency With Myopathy And Neuropathy (2) · VLCAD deficiency (2) · Carbohydrate Metabolism, Inborn Errors (1) · Carnitine Palmitoyltransferase II Deficiency, Late-Onset (1) · Carnitine palmitoyl transferase 2 deficiency (1) · Chanarin-Dorfman Syndrome (1) · Dimauro disease (1) · Glycogen Storage Disease Type II (1) · Glycogen Storage Disease Type III (1) · Glycogen Storage Disease Type IV (1) · Glycogen Storage Disease Type Ix (1) · Glycogen Storage Disease Type V (1) · Glycogen Storage Disease Type VII (1) · Glycogen Storage Disease XIII (1)
Amino Acid Metabolism, Inborn Errors (1) · Brain Diseases (1) · Brain Diseases, Metabolic (1) · Brain Diseases, Metabolic, Inborn (1) · Central Nervous System Diseases (1) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1) · Genetic Diseases, Inborn (1) · Glycogen Storage Disease (1) · Lipid Metabolism Disorders (1) · Lysosomal Storage Diseases (1) · Lysosomal Storage Diseases, Nervous System (1) · Metabolic Diseases (1) · Mitochondrial Diseases (1) · Muscular Diseases (1) · Muscular Disorders, Atrophic (1)
Exercise Test (1) · Glycerol (1) · Heparin (1) · Sodium Chloride (1) · Sugars (1) · soybean oil, phospholipid emulsion (1)
Copenhagen University Hospital, Rigshospitalet (1) · Oregon Health and Science University (1) · University Hospital, Ghent (1) · University Medical Center Groningen (1) · University of Copenhagen (1)
Denmark (2) · Belgium (1) · Netherlands (1) · United States (1)
Andreas M Fritzen, Associate Professor (1) · Karen L Madsen, MD (1) · Patrick Verloo, MD (1) · Terry Derks, MD, PhD (1)