Clinical Trials on Barth Syndrome

Total 7 results

  • NCT05554835
    Recruiting
    Conditions: Mitochondrial Diseases, Kearns-Sayre Syndrome, MIDD, SANDO, SCAE, NARP Syndrome, MELAS Syndrome, MERRF Syndrome, Coenzyme Q10 Deficiency, LHON, MNGIE, MIRAS, Barth Syndrome, MDS, Mitochondrial Myopathies, Leigh Syndrome, Pearson Syndrome, CPEO
  • NCT03098797
    Completed
    Conditions: Barth Syndrome
  • NCT01461304
    No longer available
    Conditions: 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
  • NCT04689360
    Available
    Conditions: Mitochondrial Diseases, Barth Syndrome
  • NCT01625663
    Completed
    Conditions: Barth Syndrome
  • NCT01629459
    Completed
    Conditions: Barth Syndrome
  • NCT01194141
    Completed
    Conditions: Barth Syndrome