3 completed, 1 enrolling by invitation, 1 unknown. 5 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 5 | Completed 3, Enrolling by invitation 1, Unknown 1 |
Follow VLCAD deficiency: new trials by email Literature Review of VLCAD deficiency trials Research Report on VLCAD 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 |
|---|---|---|---|---|---|---|
| Investigation of the Treatment of Patients With Mitochondrial Defects by Assisted Reproductive Technology Maternal spindle transfer - Pearson Syndrome, Mitochondria DNA Deletion | Not applicable | Enrolling by invitation | Taipei Fertility Center | 6 | 2025-04-03 | 2026-11-02 |
| Acute Nutritional Ketosis in VLCAD Deficiency ketone ester drink, exercise, muscle biopsy - VLCAD Deficiency, Fatty Acid Oxidation Defects | Not applicable | Completed | University Medical Center Groningen | 5 | 2016-04-01 | 2018-05-21 |
| 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 |
| Nutritional Therapy of the Deficits of Oxidation Mitochondrial of the Fatty Acids Oil special 107 and MYGLIOL 810 - Inborn Errors of Metabolism | Not applicable | Completed | Assistance Publique - Hôpitaux de Paris | 20 | 2006-06-01 | 2011-02-17 |
Medium chain acyl CoA dehydrogenase deficiency (2) · Metabolism, Inborn Errors (2) · Trifunctional Protein Deficiency With Myopathy And Neuropathy (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)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities (2) · Genetic Diseases, Inborn (2) · Metabolic Diseases (2) · Nutritional and Metabolic Diseases (2) · Amino Acid Metabolism, Inborn Errors (1) · Brain Diseases (1) · Brain Diseases, Metabolic (1) · Brain Diseases, Metabolic, Inborn (1) · Central Nervous System Diseases (1) · Glycogen Storage Disease (1) · Lipid Metabolism Disorders (1) · Lysosomal Storage Diseases (1) · Lysosomal Storage Diseases, Nervous System (1) · Mitochondrial Diseases (1) · Muscular Diseases (1)
Exercise (1) · Glycerol (1) · Heparin (1) · Magnetic Resonance Imaging (1) · Positron-Emission Tomography (1) · Sodium Chloride (1) · Sugars (1) · soybean oil, phospholipid emulsion (1)
Assistance Publique - Hôpitaux de Paris (1) · Copenhagen University Hospital, Rigshospitalet (1) · Oregon Health and Science University (1) · Taipei Fertility Center (1) · University Medical Center Groningen (1)
Denmark (1) · France (1) · Netherlands (1) · Taiwan (1) · United States (1)
Guy Touati, PU-PH (1) · Jeroen AL Jeneson, PhD (1) · Karen L Madsen, MD (1)