Clinical Trials on Arthrogryposis Multiplex Congenita
Total 16103 results
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Uppsala UniversityUnknownEpidermolysis Bullosa SimplexSweden
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Boston Children's HospitalRecruitingGenetic Disease | Chopra-Amiel-Gordon Syndrome | CAGS | ANKRD17United States
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Freeman-Sheldon Research Group, Inc.TerminatedDepressive Disorder | Craniofacial Abnormalities | Posttraumatic Stress Disorder | ArthrogryposisUnited States, Guatemala
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ArQule, Inc. (a wholly owned subsidiary of Merck...No longer availableGrowth Disorders | Proteus Syndrome | PIK3CA-Related Overgrowth Spectrum (PROS)
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Children's Healthcare of AtlantaTerminated
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Kamari Pharma LtdRecruitingPachyonychia Congenita | Punctate Palmoplantar Keratoderma Type 1United Kingdom
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Kamari Pharma LtdRecruitingPachyonychia Congenita | Punctate Palmoplantar Keratoderma Type 1Israel
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National Human Genome Research Institute (NHGRI)Children's National Research Institute; Uniformed Services University of the...RecruitingProteus Syndrome | PIK3CA Related Overgrowth SpectrumUnited States
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Mayo ClinicRecruitingAutosomal Dominant Polycystic Kidney | Autosomal Dominant Polycystic Liver Disease | Renal Cyst | Hepatic CystUnited States
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Mayo ClinicNot yet recruitingFamily Members | Amniocentesis Affecting Fetus or Newborn | Multiple Anomalies of Fetus | Genetic Predisposition SuspectedUnited States
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Glostrup University Hospital, CopenhagenUnknownOptic Atrophy, Autosomal DominantDenmark
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Northwestern UniversityChicago Run; American Academy of Cerebral Palsy and Developmental Medicine; Spencer...Enrolling by invitationCerebral Palsy | Gross Motor Development Delay | Motor Skills Disorders | Myelomeningocele | ArthrogryposisUnited States
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Merck Sharp & Dohme LLCActive, not recruitingPIK3CA-Related Overgrowth Spectrum (PROS)/Proteus Syndrome (PS)United States, Australia, Brazil, Italy, United Kingdom
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ArQule, Inc. (a wholly owned subsidiary of Merck...Worldwide Clinical TrialsTerminatedPIK3CA-Related Overgrowth Spectrum (PROS)/Proteus SyndromeUnited States, Australia, Italy, Spain
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ProQR TherapeuticsActive, not recruitingEye Diseases | Retinitis | Eye Diseases, Hereditary | Retinal Dystrophies | Vision Disorders | Retinal Disease | Autosomal Dominant Retinitis Pigmentosa | Vision TunnelUnited States
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National Human Genome Research Institute (NHGRI)CompletedPolydactyly | Malformations | Multiple AbnormaliesUnited States, Turkey
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Indiana UniversityRecruitingCongenital Heart Defects | Heterotaxy SyndromeUnited States
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Centers for Disease Control and PreventionInternational Centre for Diarrhoeal Disease Research, Bangladesh; Ministry...CompletedMeasles | Rubella | Rubella Syndrome, CongenitalBangladesh
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Nemours Children's ClinicCompletedMuscular Dystrophy | Spinal Muscular Atrophy | Arthrogryposis
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National Heart, Lung, and Blood Institute (NHLBI)CompletedPentalogy of CantrellUnited States
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Northwestern UniversityIcahn School of Medicine at Mount SinaiCompletedNetherton Syndrome | Ichthyosis | Lamellar Ichthyosis | Autosomal Recessive Congenital Ichthyosis | Congenital Ichthyosiform Erythroderma | Epidermolytic IchthyosisUnited States
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Stanford UniversityCompletedMarfan SyndromeUnited States
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Carelon ResearchNational Heart, Lung, and Blood Institute (NHLBI); National Institutes of Health...CompletedDown Syndrome | Congenital Heart DiseaseUnited States, Canada
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National Heart, Lung, and Blood Institute (NHLBI)Completed
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Daiichi Sankyo, Inc.CompletedNetherton SyndromeUnited States
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Daiichi Sankyo, Inc.Completed
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University of AarhusUnknownPseudohypoparathyroidism | Idiopathic Hypoparathyroidism | Autosomal Dominant HypocalcaemiaDenmark
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Ziauddin UniversityCompleted
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Northwestern UniversityIcahn School of Medicine at Mount Sinai; Galderma R&DRecruiting
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University of ZurichCompletedLeft Ventricular Noncompaction | Isolated Noncompaction of the Ventricular MyocardiumSwitzerland
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National Human Genome Research Institute (NHGRI)CompletedCoronary Artery Disease | Proteus Syndrome | Familial Isolated Hyperparathyroidism | Coffin - Sins Syndrome | Dubouitz SyndromeUnited States
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University Hospital, AntwerpUniversity Hospital, GhentRecruitingMarfan Syndrome | FBN1 MutationBelgium
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Baylor College of MedicineSouthern Star Research Pty Ltd.Recruiting
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University Hospital, GhentAgentschap voor Innovatie door Wetenschap en TechnologieCompleted
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Atılım UniversityCompletedDown Syndrome | Gross Motor Development Delay | Congenital Heart DefectsTurkey
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Stanford UniversityMidwestern UniversityCompletedMarfan SyndromeUnited States
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Ann & Robert H Lurie Children's Hospital of ChicagoJohns Hopkins UniversityWithdrawnMarfan SyndromeUnited States
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University of OxfordOxford University Hospitals NHS TrustUnknown
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Brigham and Women's HospitalBoston Children's HospitalCompletedMarfan SyndromeUnited States
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Academisch Medisch Centrum - Universiteit van Amsterdam...Netherlands Organisation for Scientific ResearchRecruiting
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University Hospital, ToulouseNot yet recruiting
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French Cardiology SocietyCompleted
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Assistance Publique - Hôpitaux de ParisHospices Civils de Lyon; Banque de cellules cochinCompleted
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University of British ColumbiaHeart and Stroke Foundation of CanadaCompleted
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University of AlbertaCompletedHeterotaxy SyndromeCanada
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University of OklahomaCompletedCerebral Palsy | Spinal Muscular Atrophy | Arthrogryposis | Other Central Nervous System or Musculoskeletal DisordersUnited States
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Quoin PharmaceuticalsRecruitingNetherton SyndromeUnited States
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University Hospital, ToulouseRecruiting
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Baylor College of MedicineThe Marfan FoundationCompleted
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University Hospital, ToulouseCompleted