97 studies found for:    "Mitochondrial Diseases" OR "mitochondrial neurogastrointestinal encephalopathy disease"
Show Display Options
Rank Status Study
21 Completed Economic and Medical Evaluation of the Whole Mitochondrial DNA Screening by Surveyor and Mitochips Techniques
Condition: Mitochondrial Disease
Intervention:
22 Completed Responses to Influenza Vaccine in Patients With Mitochondrial Disorders (MELAS)
Condition: MELAS Syndrome
Intervention: Biological: Intramuscular seasonal trivalent inactivated influenza vaccine
23 Completed Therapy for Chronic Fatigue Syndrome: A Presumptive Mitochondrial Disorder
Condition: Chronic Fatigue Syndrome
Intervention: Drug: Nutraceuticals
24 Recruiting Natural History Study - Mitochondrial Disease
Condition: Mitochondrial DNA Mutation
Intervention:
25 Completed Mitochondria and Metabolic Syndrome in a Southern California Chinese Cohort
Conditions: Metabolic Syndrome;   Type 2 Diabetes Mellitus
Intervention: Device: Diffuse Optical Spectroscopy
26 Not yet recruiting Chronic Fatigue Syndrome: A Presumptive Mitochondrial Disorder
Condition: Chronic Fatigue Syndrome
Interventions: Drug: Nutraceutical supplements;   Drug: Placebo
27 Active, not recruiting EPI-743 for Metabolism or Mitochondrial Disorders
Conditions: Metabolic Disease;   Neurology;   Myoptahy
Intervention: Drug: EPI-743
28 Not yet recruiting Phase 2 Study of EPI-743 in Children With Pearson Syndrome
Condition: Pearson Syndrome
Intervention: Drug: EPI-743
29 Unknown  Evaluating the Effectiveness of a Dichloroacetate in MELAS Syndrome
Condition: MELAS Syndrome
Intervention: Drug: Dichloroacetate
30 Active, not recruiting Safety and Efficacy Study of EPI-743 in Children With Leigh Syndrome
Condition: Leigh Syndrome
Interventions: Drug: Placebo;   Drug: EPI-743 15 mg/kg;   Drug: EPI-743 5 mg/kg
31 Completed Abdominal Adiposity and Muscle Mitochondrial Functions
Condition: Mitochondrial Respiratory Chain Deficiencies
Intervention:
32 Completed High Protein Diet in Patients With Long-chain Fatty Acid Oxidation Disorders
Conditions: Very Long-chain Acyl-CoA Dehydrogenase Deficiency;   Trifunctional Protein Deficiency;   Carnitine Palmitoyltransferase 2 Deficiency;   Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
Intervention: Behavioral: Diet counseling
33 Recruiting Study of Dapagliflozin on Mitochondrial Dysfunction and Impaired Insulin Signaling/Action
Conditions: Insulin Sensitivity;   Multiple Mitochondrial Dysfunctions Syndrome
Interventions: Drug: Dapagliflozin;   Drug: Placebo
34 Unknown  Assessing Immune Function in Young Patients With Cytopenia That Did Not Respond to Treatment
Conditions: Dyskeratosis Congenita;   Fanconi Anemia;   Myelodysplastic Syndromes;   Nonmalignant Neoplasm;   Pearson Marrow-pancreas Syndrome;   Shwachman-diamond Syndrome
Interventions: Genetic: polymerase chain reaction;   Other: flow cytometry;   Other: immunologic technique;   Procedure: biopsy
35 Completed Effect of Bezafibrate on Muscle Metabolism in Patients With Fatty Acid Oxidation Defects
Conditions: Carnitine Palmitoyltransferase II Deficiency;   Very Long Chain Acyl Coa Dehydrogenase Deficiency
Interventions: Drug: Bezafibrate;   Other: Placebo
36 Completed Efficacy of Epoetin Alfa in Patients With Friedreich's Ataxia
Condition: Friedreich's Ataxia
Intervention: Drug: Epoetin alfa
37 Completed Transcorneal Electrical Stimulation Therapy for Retinal Disease
Conditions: Retinitis Pigmentosa;   Macula Off;   Primary Open Angle Glaucoma;   Hereditary Macular Degeneration;   Treated Retina Detachment;   Retinal Artery Occlusion;   Retinal Vein Occlusion;   Non-Arthritic-Anterior-Ischemic Optic-Neuropathy;   Hereditary Autosomal Dominant Optic Atrophy;   Dry Age Related Macular Degeneration;   Ischemic Macula Edema
Interventions: Device: Transcorneal Electrical Stimulation;   Device: DTL-electrode attached without energy
38 Completed
Has Results
Fatty Acid Oxidation Disorders & Body Weight Regulation Grant
Condition: Trifunctional Protein Deficiency
Intervention:
39 Available Compassionate Use of Triheptanoin (C7) for Fatty Acid Oxidation Disorders and Glycogen Storage Disease
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, Type B;   Acyl-coA Dehydrogenase, Type 9
Intervention: Drug: triheptanoin
40 Completed Patient Reported Outcomes in Friedreich's Ataxia Patients After Withdrawal From Treatment With Idebenone (PROTI)
Condition: Friedreich's Ataxia
Intervention: Drug: Idebenone

Show previous page of results Previous Page (1-20) Studies Shown (21-40) Next Page (41-60) Show next page of results
Indicates status has not been verified in more than two years