Page 1 of Clinical Trials for Muscle, 5259 Total Matches
- 1RecruitingLast Updated: September 1, 2011Condition(s): Pelvic Floor; Pelvic Floor Dysfunction; Pelvic Floor Muscle Injury
- 2CompletedLast Updated: December 26, 2008Condition(s): Diabetes Complications; Inspiratory Muscle Weakness
- 3RecruitingLast Updated: March 6, 2008Condition(s): Heart Failure
- 4Active, not recruitingLast Updated: October 13, 2011Condition(s): Normal Healthy Subjects
- 5RecruitingLast Updated: June 23, 2010Condition(s): Critical Illness; Septic Shock; Trauma; Acute Organ Failure
- 6RecruitingLast Updated: June 30, 2011Condition(s): Inspiratory Muscle Training; Stem Cell Transplantation; Respiratory Muscle Training
- 7CompletedLast Updated: February 24, 2012Condition(s): Muscle Strength Quantitative Trait Locus 1
- 8RecruitingLast Updated: April 8, 2012Condition(s): Muscle Relaxation; Muscle Trauma; Analgetic Consumption; Total Hip Replacement
- 9RecruitingLast Updated: May 25, 2011Condition(s): Urinary Incontinence
- 10Active, not recruitingLast Updated: November 27, 2009Condition(s): Muscle Quadriceps Femoris; Healthy
- 11RecruitingLast 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
- 12CompletedLast Updated: March 22, 2012Condition(s): Muscular Dystrophies
- 13RecruitingLast Updated: May 9, 2012Condition(s): Facioscapulohumeral Muscular Dystrophy
- 14RecruitingLast Updated: September 12, 2011Condition(s): Myositis; Polymyositis; Dermatomyositis; Myositis, Inclusion Body
- 15Enrolling by invitationLast Updated: January 4, 2012Condition(s): Amyotrophic Lateral Sclerosis
- 16CompletedLast Updated: March 31, 2008Condition(s): Urinary Incontinence
- 17RecruitingLast Updated: August 11, 2011Condition(s): Intensive Care Unit Acquired Paresis; Muscle Wasting
- 18RecruitingLast Updated: February 1, 2012Condition(s): Muscular Dystrophy, Duchenne
- 19CompletedLast Updated: April 15, 2010Condition(s): Skeletal Muscle Ultrasound; Isometric Muscle Strength
- 20Completed
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?term=Muscle
