Search clinical trials for: Natural History
Total 4194 results
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Indiana UniversityAcademic Model Providing Access to Healthcare (AMPATH)Not yet recruitingCervical Cancer | Cervical Cancer Prevention
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Massachusetts General HospitalRecruitingRecurrent Respiratory Papillomatosis | Pulmonary NeoplasmUnited States
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University of Missouri-ColumbiaRecruitingEpilepsy, Generalized | Sleep Disorder | Rare Diseases | Development Delay | Motor Delay | Autism or Autistic Traits | SYT-SSX Fusion Protein ExpressionUnited States
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Imagine InstituteNot yet recruitingDevelopmental and Epileptic Encephalopathy
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National Cancer Institute (NCI)Recruiting
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Clinic for Special ChildrenRecruitingMyopathy | Myopathy; Hereditary | Myopathies, Nemaline | TNNT1-associated Myopathy | Infantile-onset Nemaline Rod Myopathy | Myopathy, Rod | Amish Nemaline Myopathy | Nemaline Myopathy 5 | NEM5 | Genetic Muscle Disease | Recessive Hereditary Disorder (Autosomal) | ANMUnited States
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Fondazione Policlinico Universitario Agostino Gemelli...RecruitingDuchenne Muscular Dystrophy | Natural History | Motor Function; RetardationItaly
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Institut de Myologie, FranceAssociation Française contre les Myopathies (AFM), ParisNot yet recruitingMerosin Deficient Congenital Muscular DystrophyFrance
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University Hospital TuebingenRecruitingRetinitis PigmentosaGermany
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Hospices Civils de LyonNot yet recruitingSpinal Muscular AtrophyFrance
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National Taiwan University HospitalRecruiting
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Istituto Auxologico ItalianoUniversity of Turin, ItalyRecruiting
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National Institute of Nursing Research (NINR)Not yet recruitingRyanodine Receptor 1-Related Myopathy | Ryanodine Receptor 1 Related DisordersUnited States
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University College, LondonUniversity of North Carolina, Chapel Hill; NYU Grossman School of MedicineRecruitingDentatorubral-Pallidoluysian AtrophyUnited States, United Kingdom
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Centre Hospitalier Universitaire de LiegeCentre Hospitalier Régional de la Citadelle; SYSNAVRecruitingAngelman SyndromeBelgium
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University of Maryland, BaltimoreNot yet recruitingPain | Virtual Reality | Temporomandibular Disorder | PlaceboUnited States
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University of PennsylvaniaRecruitingLCAT DeficiencyUnited States
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Rocket Pharmaceuticals Inc.Recruiting
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Atamyo TherapeuticsNot yet recruiting
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McGill University Health Centre/Research Institute...Canadian Institutes of Health Research (CIHR)RecruitingZellweger Spectrum DisorderCanada
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Insel Gruppe AG, University Hospital BernRecruiting
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Radboud University Medical CenterUMC UtrechtNot yet recruitingCentronuclear Myopathy | Nemaline Myopathy | Central Core Disease | Multi-Minicore DiseaseNetherlands
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Elpida Therapeutics SPCNot yet recruitingNeuromuscular Diseases | Peripheral Neuropathy | Neuro-Degenerative Disease
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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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PYC TherapeuticsNot yet recruitingOptic Atrophies, Hereditary | Autosomal Dominant Optic Atrophy | Optic Atrophy, Autosomal Dominant | Kjer Optic AtrophyAustralia
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Radboud University Medical CenterRecruitingSELENON-related Myopathy | LAMA2-related Muscular DystrophyNetherlands
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Baylor College of MedicineGrace Science FoundationRecruiting
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Puerta de Hierro University HospitalParc Taulí Hospital UniversitariRecruiting
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National Human Genome Research Institute (NHGRI)RecruitingMetabolic Disease | Purine-Pyrimidine Metabolism | AICDA, OMIM *605257, Immunodeficiency With Hyper-IgM, Type 2; HIGM2 | UNG, OMIM *191525, Hyper-IgM Syndrome 5 | NT5C3A<TAB>, OMIM *606224, Anemia, Hemolytic, Due to UMPH1 Deficiency | UMPS, OMIM *613891, Orotic Aciduria | DHODH, OMIM *126064,... and other conditionsUnited States
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Centre Hospitalier Universitaire de NiceRecruitingFacioscapulohumeral Muscular Dystrophy Type 2France, Italy, Spain
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argenxRecruitingCongenital Myasthenic SyndromeSpain, France, United States, Canada
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National Alliance for Sickle Cell CentersBeam Therapeutics Inc.RecruitingSickle Cell TraitUnited States
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China National Center for Cardiovascular DiseasesNot yet recruitingCoronary Artery Disease Progression | Optical Coherence Tomography | Atherosclerotic Lesion | Radial Wall Strain
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Fondazione Policlinico Universitario Agostino Gemelli...RecruitingDiarrhea | Gastroesophageal Reflux | Functional Gastrointestinal Disorders | Constipation - Functional | Colic, Infantile | Dyschezia | Vomiting; CyclicalItaly
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Regeneron PharmaceuticalsRecruitingCongenital Hearing Loss Secondary to Biallelic Mutations in the Otoferlin Gene (OTOF) | Biallelic Mutations in the Gap Junction Beta 2 (GJB2) Gene | Digenic Mutations in GJB2/Gap Junction Beta 6 (GJB6) GenesUnited States
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Eunice Kennedy Shriver National Institute of Child...RecruitingEpilepsy | Obesity | Intellectual Disability | Microcephaly | Nervous System Malformations | HypogonadismsUnited States
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Friedreich's Ataxia Research AllianceRecruitingFriedreich AtaxiaUnited States, Canada, New Zealand, Australia, France, Austria, Belgium, Brazil, Czechia, Germany, Greece, Ireland, Italy, Spain, United Kingdom, India, Netherlands
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Royal College of Surgeons, IrelandThe Hospital for Sick Children; Massachusetts General Hospital; Belfast Health... and other collaboratorsNot yet recruiting
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PfizerRecruitingCardiomyopathy, Dilated | Bcl-2 Anathogene-3 (BAG3) Dilated Cardiomyopathy (DCM)United States, Spain, Netherlands, Poland, United Kingdom
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National Cancer Institute (NCI)RecruitingAcute Lymphoblastic Leukemia | Relapsed/Refractory | B CellUnited States
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Massachusetts General HospitalNorthwestern University; University of Florida; University of Minnesota; Henry... and other collaboratorsRecruitingALS | Kennedy Disease | MND (Motor Neurone DIsease) | PLS | PMA - Progressive Muscular Atrophy | PBP - Progressive Bulbar PalsyUnited States, Italy
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Tobias MoserRecruitingHearing Impairment | Otoferlin-related Auditory SynaptopathyGermany
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Johan VirhammarSwedish Society for Medical ResearchRecruitingHydrocephalus | Normal Pressure HydrocephalusSweden, Finland, Italy
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Hereditary Neuropathy FoundationRecruitingCharcot-Marie-Tooth Disease | Charcot-Marie-Tooth Disease, Type IA | Charcot-Marie-Tooth Disease Type 2A | Charcot-Marie-Tooth | Charcot-Marie-Tooth Disease, Type IB | Charcot-Marie-Tooth Disease Type 2 | Charcot-Marie-Tooth Disease, Type 2C | Charcot-Marie-Tooth Disease Type 2A2B | Charcot-Marie-Tooth... and other conditionsUnited States
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Wake Forest University Health SciencesRecruitingHemorrhagic Stroke | Acute Ischemic StrokeUnited States
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Ambulanzpartner Soziotechnologie APST GmbHCharite University, Berlin, GermanyRecruitingMotor Neuron Disease, Amyotrophic Lateral SclerosisGermany
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University of California, San DiegoNew York University; Heinrich-Heine University, Duesseldorf; Universität TübingenRecruitingGenetic Disease | Mitochondrial Encephalomyopathies | Neonatal Encephalopathy | Mutation | Hereditary Spastic Paraplegia | White Matter Disease | Spastic ParaplegiaUnited States
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Phoenix NestAparito Ltd.; Vaincres Les Maladies Lysosomales; Association Sanfilippo SudNot yet recruitingSanfilippo Syndrome Type CUnited States, France
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Columbia UniversityNational Eye Institute (NEI); Centre Hospitalier National d'Ophtalmologie des... and other collaboratorsRecruitingRetinitis Pigmentosa | Best Vitelliform Macular DystrophyUnited States, Germany, France