Page 1 of Clinical Trials for "Muscular Diseases", 955 Total Matches
- 1RecruitingLast Updated: July 28, 2011Condition(s): Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; 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 Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy
- 2RecruitingLast Updated: June 22, 2011Condition(s): Central Core Disease; Centronuclear Myopathy; Congenital Fiber Type Disproportion; Multiminicore Disease; Myotubular Myopathy; Nemaline Myopathy; Rigid Spine Muscular Dystrophy; Undefined Congenital Myopathy
- 3RecruitingLast Updated: May 21, 2012Condition(s): GNE Myopathy; Hereditary Inclusion Body Myopathy
- 4RecruitingLast Updated: May 12, 2011Condition(s): Inclusion Body Myopathy With Early-onset Paget Disease and Frontotemporal Dementia; Paget Disease of Bone; Frontotemporal Dementia; Myopathy
- 5CompletedLast Updated: September 7, 2011Condition(s): Nonaka Myopathy; Hereditary Inclusion Body Myopathy
- 6Active, not recruitingLast Updated: April 17, 2012Condition(s): Bethlem Myopathy; Ullrich Congenital Muscular Dystrophy
- 7Recruiting
- 8RecruitingLast Updated: January 8, 2012Condition(s): Brain Injuries; Dementia; Myopathies; Muscle Disorders
- 9Recruiting
- 10Active, not recruitingLast Updated: December 20, 2011Condition(s): Myopathy; Cognitive Impairment
- 11RecruitingLast Updated: October 24, 2007Condition(s): Rhabdomyolysis; Myopathy
- 12CompletedLast Updated: March 21, 2012Condition(s): Hereditary Inclusion Body Myopathy
- 13RecruitingLast Updated: March 14, 2012Condition(s): Hereditary Inclusion Body Myopathy
- 14RecruitingLast Updated: May 17, 2012Condition(s): Muscular Dystrophies; Muscle Myopathies; Hereditary Spastic Paraplegias; Inherited Neuropathies; Inherited Neuromuscular Conditions
- 15RecruitingLast Updated: May 18, 2009Condition(s): Mitochondrial Myopathy
- 16RecruitingLast Updated: April 9, 2012Condition(s): MYOPATHY
- 17Active, not recruitingLast Updated: November 4, 2011Condition(s): Statin-Associated Myopathy
- 18RecruitingLast Updated: August 12, 2011Condition(s): Idiopathic Inflammatory Myopathy
- 19RecruitingLast Updated: June 29, 2011Condition(s): Statin Myopathy
- 20RecruitingLast Updated: October 24, 2011Condition(s): Myopathy (Statin Associated)
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The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Muscular+Diseases%22
