Clinical Trials on Congenital Muscular Dystrophy

Total 17 results





    • NCT01805024
      Completed
      Conditions: Congenital Muscular Dystrophy
    • NCT01836627
      Completed
      Conditions: Congenital Muscular Dystrophy
    • NCT04299321
      Recruiting
      Conditions: Merosin Deficient Congenital Muscular Dystrophy
    • NCT01952028
      Withdrawn
      Conditions: LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A)
    • NCT02153970
      Completed
      Conditions: Cerebral Palsy; Neuromuscular Disease
    • NCT01438788
      Completed
      Conditions: Bethlem Myopathy; Ullrich Congenital Muscular Dystrophy
    • NCT03970135
      Completed
      Conditions: Spinal Muscular Atrophy; Merosin Deficient Congenital Muscular Dystrophy
    • NCT01422200
      Completed
      Conditions: Duchenne Muscular Dystrophy; Spinal Muscular Atrophy; Congenital Muscular Dystrophy
    • NCT04478981
      Recruiting
      Conditions: MDC1A; SELENON-related 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)
    • NCT04020159
      Recruiting
      Conditions: Bethlem Myopathy; Ullrich Congenital Muscular Dystrophy 1, Digenic, Col6A1/Col6A2; Ullrich Congenital Muscular Dystrophy 1, Autosomal Recessive; Ullrich Congenital Muscular Dystrophy 1, Autosomal Dominant; Bethlem Myopathy 1, Autosomal Recessive; UCMD; BTHLM1
    • NCT04001595
      Recruiting
      Conditions: LGMD2I; LGMDR9; Limb Girdle Muscular Dystrophy; Congenital Muscular Dystrophy; Muscle-Eye-Brain Disease; Walker-Warburg Syndrome; FKRP Gene Mutation
    • NCT00313677
      Recruiting
      Conditions: Muscular Dystrophy
    • 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
    • NCT00082108
      Recruiting
      Conditions: Myotonic Dystrophy; Facioscapulohumeral Muscular Dystrophy; Muscular Dystrophy; Myotonic Dystrophy Type 1; Myotonic Dystrophy Type 2; Congenital Myotonic Dystrophy; PROMM (Proximal Myotonic Myopathy); Steinert's Disease; Myotonic Muscular Dystrophy
    • NCT03692312
      Not yet recruiting
      Conditions: Congenital Myotonic Dystrophy
    • NCT03059264
      Suspended
      Conditions: Congenital Myotonic Dystrophy