Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting
5 studies found for:    "Barth syndrome"
Show Display Options
Rank Status Study
1 Completed Exercise Training in Barth Syndrome
Condition: Barth Syndrome
Intervention: Behavioral: Exercise training
2 Recruiting Resistance Exercise in Barth Syndrome
Condition: Barth Syndrome
Intervention: Behavioral: Resistance exercise and protein supplementation
3 Recruiting Heart and Muscle Metabolism in Barth Syndrome
Condition: Barth Syndrome
Intervention:
4 Available Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism
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
Intervention: Drug: triheptanoin
5 Recruiting North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)
Conditions: Mitochondrial Disorders;   Mitochondrial Genetic Disorders;   Mitochondrial Diseases;   Disorder of Mitochondrial Respiratory Chain Complexes;   Deletion and Duplication of Mitochondrial DNA
Intervention:

Indicates status has not been verified in more than two years