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Clinical Trials on Mitochondrial Genetic Disorders
Total 151614 results
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Erin RothwellNational Human Genome Research Institute (NHGRI)RecruitingPregnancy | Shared Decision Making | Genetic Testing | Genetic Counseling | Prenatal DisorderUnited States
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Imperial College London Diabetes CentreUnknownMendelian Disorders | Genetic Disorder | Novel Mutation | Hereditary Disorder | De Novo Mutation | Inherited Disease | Single-Gene DefectsUnited Arab Emirates
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PTC TherapeuticsCompletedLeigh SyndromeUnited States
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Aadi Bioscience, Inc.Withdrawn
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Spark TherapeuticsCompletedHematologic Diseases | Hemophilia A | Blood Coagulation Disorders, Inherited | Coagulation Protein Disorders | Hemorrhagic Disorders | Genetic Diseases, Inborn | Genetic Diseases, X-Linked | Blood Coagulation Disorder | Factor VIII DeficiencyUnited States, Australia, Thailand, Canada
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Centre Hospitalier National d'Ophtalmologie des...StreetlabCompletedRetinitis Pigmentosa | Leber's Hereditary Optic Neuropathy | Stargardt DiseaseFrance
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Bin LiHuazhong University of Science and TechnologyCompletedLeber Hereditary Optic NeuropathyChina
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Glostrup University Hospital, CopenhagenUnknownOptic Atrophy, Autosomal DominantDenmark
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Oregon Health and Science UniversityUniversity of PittsburghCompletedVery Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency | Carnitine Palmitoyltransferase 2 (CPT2) Deficiency | Mitochondrial Trifunctional Protein (TFP) Deficiency | Long-chain 3 hydroxyacylCoA Dehydrogenase (LCHAD) DeficiencyUnited States
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Boston Children's HospitalBoston Medical Center; National Human Genome Research Institute (NHGRI); The... and other collaboratorsRecruitingGenetic Predisposition to Disease | Genetics Disease | Genetics/Birth DefectsUnited States
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LMU KlinikumSeventh Framework Programme; NBIA AllianceRecruitingNeurodegeneration With Brain Iron Accumulation (NBIA) | Pantothenate Kinase-associated Neurodegeneration (PKAN) | Aceruloplasminemia | Beta-Propeller Protein-Associated Neurodegeneration (BPAN) | Mitochondrial Membrane Protein Associated Neurodegeneration (MPAN) | Fatty Acid Hydroxylase-associated... and other conditionsCanada, Czechia, Germany, Italy, Netherlands, Poland, Serbia, Spain
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Argo SanteGenSight BiologicsCompleted
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Oklahoma Medical Research FoundationUniversity of Wisconsin, Madison; University of Oklahoma; National Institute...RecruitingInsulin Resistance | Chronic Disease | Aging | Insulin Sensitivity | MitochondriaUnited States
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University Hospital, Strasbourg, FranceUnknownGenetic Disorders in PregnancyFrance
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Natera, Inc.Ferring PharmaceuticalsTerminatedIn Vitro Fertilization (IVF) | Preimplantation Genetic Diagnosis (PGD) | Preimplantation Gentic Screening (PGS)United States
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BioMarin PharmaceuticalUnknownRare Genetic DisordersUnited States
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Kaiser PermanenteNational Human Genome Research Institute (NHGRI)CompletedGenetic DisordersUnited States
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Abbott MolecularUnknown
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University Hospital, GhentCompletedGenetic Disease | Embryo | Embryo DisorderBelgium
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University of California, IrvineWithdrawnDilated Cardiomyopathy | Hypertrophic Cardiomyopathy | Restrictive Cardiomyopathy | Mitochondrial Cardiomyopathy | Noncompaction CardiomyopathyUnited States
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Novo Nordisk A/SCompletedPrader-Willi Syndrome | Genetic DisorderGermany, Denmark, Switzerland
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University of AarhusAarhus University HospitalNot yet recruitingHeart Failure | Ischemia Reperfusion Injury | Mitochondrial PathologyDenmark
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TESS Research FoundationBrown University; Stanford University; University of Texas Southwestern Medical...RecruitingEpilepsy | Movement Disorders | Rare Diseases | Genetic Disorder | Citrate Transporter Deficiency | SLC13A5 Deficiency | EIEE25 | Kohlschutter-Tonz Syndrome (Non-ROGDI) | Citrate Transporter Disorder | DEE25United States
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Boston Children's HospitalRecruitingGenetic Predisposition to Disease | Genetic Disease | Development, Infant | Genetic Syndrome | Development, ChildUnited States
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Second Affiliated Hospital, School of Medicine,...CompletedPlasma microRNA in Patients With Genetic Susceptibility to Mental Disorders
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University of Maryland, BaltimoreNational Institute of Nursing Research (NINR)CompletedPain | Physical Activity | Osteoarthritis, Knee | Mitochondrial PathologyUnited States
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Weill Medical College of Cornell UniversityNational Heart, Lung, and Blood Institute (NHLBI)RecruitingMyocardial Fibrosis | Cardiomyopathies | Friedreich Ataxia | Cardiac HypertrophyUnited States
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Rady Pediatric Genomics & Systems Medicine InstituteEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsActive, not recruitingGenetic Diseases | Genetic Syndrome | Mendelian DisordersUnited States
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The Hospital for Sick ChildrenRecruitingGenetic Disease | Inherited DiseaseCanada
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National Human Genome Research Institute (NHGRI)CompletedHereditary DiseasesUnited States
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National Institute of Environmental Health Sciences...Massachusetts General HospitalRecruitingInfertility | Hypogonadism | Amenorrhea | Genetic DisorderUnited States
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Cliniques universitaires Saint-Luc- Université...RecruitingIschemia Reperfusion Injury | Kidney Transplant; Complications | Delayed Graft Function | MitochondrialBelgium
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Murdoch Childrens Research InstituteUniversity of Sydney; Sydney Children's Hospitals Network; Women's and Children... and other collaboratorsActive, not recruitingAutosomal Recessive Disorder | X-Linked Genetic DiseasesAustralia
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Novo Nordisk A/SCompletedAchondroplasia | Genetic DisorderJapan
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Novo Nordisk A/SCompleted
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TESS Research FoundationStanford UniversityEnrolling by invitationEpilepsy | Movement Disorders | Rare Diseases | Genetic Disorder | Citrate Transporter Deficiency | SLC13A5 Deficiency | EIEE25 | Kohlschutter-Tonz Syndrome (Non-ROGDI) | 17p13.1 Deletions Confined to SLC13A5 Gene | Citrate Transporter DisorderUnited States
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Hospital Clínico Universitario de ValladolidCompletedRadiation Exposure | Cytogenetic AbnormalitySpain
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KK Women's and Children's HospitalNational University Hospital, SingaporeActive, not recruitingGenetic Predisposition | Postnatal DepressionSingapore
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National Institute on Drug Abuse (NIDA)CompletedDrug Abuse/Dependence | Genetic Underpinning of Substance Abuse | Polymorphism-genetic | Opiod-Related DisordersUnited States
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Baylor College of MedicineRecruitingObesity, Childhood | Genetic DiseaseUnited States
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Boston UniversityActive, not recruiting
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Carmel Medical CenterTechnion, Israel Institute of Technology; Soroka University Medical CenterCompleted
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Peking University People's HospitalEnrolling by invitationElderly | Infertility, Female | Mitochondrial | Assisted Reproductive TechniqueChina
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Central Hospital, Nancy, FranceUnknownGenetic Disease | IUGR | Prenatal Disorder
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University of ChicagoPfizer; Biogen; APDM Wearable TechnologiesActive, not recruitingSpinocerebellar Ataxia Type 3 | Friedreich Ataxia | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 6United States
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University of PittsburghCompletedPulmonary Hypertension | Friedreich Ataxia | Iron-sulfur Cluster DeficiencyUnited States
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University of Mississippi Medical CenterCompletedAutistic Disorder | Rett Syndrome | Asperger Syndrome | Pervasive Developmental Disorder | Childhood Disintegrative DisorderUnited States
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Affiliated Hospital of Nantong UniversityNot yet recruitingDepression | Polymerase Chain Reaction | Polymorphism, Genetic | CYP1A2 Polymorphism | Plasma Concentration | CYP2C9 Polymorphism
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Novo Nordisk A/SCompletedCongenital Bleeding Disorder | Haemophilia BUnited States, Netherlands, Austria, Spain, Germany, Macedonia, The Former Yugoslav Republic of, Taiwan, United Kingdom, Italy, Malaysia, Thailand, France, Greece, Turkey, Japan, South Africa, Romania
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Novo Nordisk A/SCompletedCongenital Bleeding Disorder | Haemophilia BUnited States, Sweden, Spain, Germany, United Kingdom, Denmark, France, Japan