Clinical Trials on Myopathy Congenital

Total 40 results

    • NCT02020187
      Completed
      Conditions: Congenital Myopathy
    • NCT04733976
      Recruiting
      Conditions: Muscular Dystrophies; Congenital Myopathy
    • NCT03018184
      Active, not recruiting
      Conditions: Inherited Muscle Diseases; Congenital Myopathy; RYR1-myopathy
    • NCT02362425
      Completed
      Conditions: Neuromuscular Disease
    • NCT00272883
      Recruiting
      Conditions: Central Core Disease; Centronuclear Myopathy; Congenital Fiber Type Disproportion; Multiminicore Disease; Myotubular Myopathy; Nemaline Myopathy; Rigid Spine Muscular Dystrophy; Undefined Congenital Myopathy
    • NCT01403402
      Unknown status
      Conditions: Congenital Muscular Dystrophy (Including Unspecified/Undiagnosed); Dystroglycanopathy; Congenital Fiber Type Disproportion; Rigid Spine Muscular Dystrophy; Congenital Myopathy (Including Unspecified/Undiagnosed); Collagen VI CMD (Ullrich CMD, Intermediate, Bethlem Myopathy); Laminin Alpha 2 Related Congenital Muscular Dystrophy; LAMA2-CMD/Merosin Deficient/MDC1A; Walker-Warburg Syndrome; Muscle-Eye-Brain Disease; Fukuyama/Fukutin Related Muscular Dystrophy; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; LMNA-CMD/Lamin A/C/Laminopathy; SEPN1-Related Myopathy; Bethlem Myopathy; Actin Aggregation Myopathy; Cap Disease; Central Core Disease; Centronuclear Myopathy; Core Rod Myopathy; Hyaline Body Myopathy; Multiminicore Myopathy; Myotubular Myopathy; Nemaline Myopathy; Tubular Aggregate Myopathy; Zebra Body Myopathy; Reducing Body Myopathy; Spheroid Body Myopathy; LGMD1B (LMNA); LGMD1E (DES); LGMD2G (TCAP); LGMD2H (TRIM32); LGMD2I (FKRP); LGMD2J (TTN); LGMD2K (POMT1); LGMD2M (FKTN); LGMD2N (POMT2); LGMD2O (POMGnT1); LGMD2P (DAG1); LGMD2Q (PLEC1); LGMD2R (DES); LGMD2S (TRAPPC11); LGMD2T (GMPPB); LGMD2U (ISPD); LGMD2V (GAA); Ullrich Congenital Muscular Dystrophy; Titinopathy; Choline Kinase B Receptor; Emery-Dreifuss Muscular Dystrophy; RYR1 Related Myopathy; SYNE1/Nesprin Related Muscular Dystrophy; Telethonin Related Muscular Dystrophy (TCAP/Titin-Cap); Congenital Myasthenic Syndrome; Escobar Syndrome; Myofibrillar Myopathy; Malignant Hyperthermia; Alpha-Dystroglycan Related Muscular Dystrophy (DAG1, DPM1, DPM2, DPM3, FKRP, FKTN); Alpha-Dystroglycan Related Muscular Dystrophy (GAA, ISPD, LARGE, POMT1, POMT2, POMGnT1); Alpha-Dystroglycan Related Muscular Dystrophy (Unspecified/Undiagnosed/Other)
    • NCT02789059
      Unknown status
      Conditions: Neuromuscular Diseases
    • NCT01817946
      Completed
      Conditions: Myotubular Myopathy
    • NCT04478981
      Recruiting
      Conditions: MDC1A; SELENON-related Myopathy
    • NCT00839033
      Terminated
      Conditions: Duchenne Muscular Dystrophy; Amyotrophic Lateral Sclerosis; Neuromuscular Diseases
    • NCT00267462
      Terminated
      Conditions: Congenital Disorders
    • NCT01438788
      Completed
      Conditions: Bethlem Myopathy; Ullrich Congenital Muscular Dystrophy
    • NCT01902940
      Completed
      Conditions: Inclusion Body Myositis, Sporadic; Inclusion Body Myopathy, Autosomal-recessive; Inclusion Body Myopathy, Autosomal-dominant; Congenital Cataracts, Facial Dysmorphism, And Neuropathy
    • NCT04743557
      Not yet recruiting
      Conditions: Centronuclear Myopathy
    • NCT01840657
      Completed
      Conditions: X-linked Myotubular Myopathy
    • NCT03351270
      Recruiting
      Conditions: Centronuclear Myopathy
    • NCT02453152
      Completed
      Conditions: X-linked Myotubular Myopathy
    • NCT02057705
      Completed
      Conditions: Myotubular Myopathy
    • NCT04033159
      Recruiting
      Conditions: Centronuclear Myopathy
    • NCT03199469
      Active, not recruiting
      Conditions: X-Linked Myotubular Myopathy
    • NCT02704273
      Completed
      Conditions: X-linked Myotubular Myopathy
    • NCT02231697
      Completed
      Conditions: Males With X-linked Myotubular Myopathy (XLMTM)
    • NCT04064307
      Recruiting
      Conditions: Myotubular Myopathy; Myotubular Myopathy 1; Myotubular (Centronuclear) Myopathy; Centronuclear Myopathy; Centronuclear Myopathy, X-Linked; X-linked Myotubular Myopathy
    • NCT02830763
      Terminated
      Conditions: Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)
    • NCT02035501
      Unknown status
      Conditions: Nemaline Myopathy