Clinical Trials on Barth Syndrome

Total 6 results





    • NCT03098797
      Active, not recruiting
      Conditions: Barth Syndrome
    • NCT01194141
      Completed
      Conditions: Barth Syndrome
    • NCT01625663
      Completed
      Conditions: Barth Syndrome
    • NCT01629459
      Completed
      Conditions: Barth Syndrome
    • NCT01461304
      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
    • NCT01694940
      Recruiting
      Conditions: Mitochondrial Disorders; Mitochondrial Genetic Disorders; Mitochondrial Diseases; Disorder of Mitochondrial Respiratory Chain Complexes; Deletion and Duplication of Mitochondrial DNA