Page 1 of Clinical Trials for "Muscle Rigidity", 42 Total Matches
- 1CompletedLast Updated: July 13, 2006Condition(s): Muscle Rigidity; Spasm; Stiff Man Syndrome
- 2Active, not recruitingLast Updated: July 21, 2011Condition(s): "Primary Open Angle Glaucoma, Ocular Hypertension"
- 3CompletedLast Updated: May 11, 2007Condition(s): Cerebral Palsy; Hypertonia; Spasticity; Dystonia; Rigidity
- 4RecruitingLast 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
- 5CompletedLast Updated: November 9, 2011Condition(s): Pleural Diseases
- 6Active, not recruitingLast Updated: June 2, 2008Condition(s): Bladder Cancer; Bladder Stones; Hematuria; Structural Abnormalities; Voiding Dysfunction
- 7Active, not recruitingLast Updated: February 14, 2011Condition(s): Pain
- 8RecruitingLast Updated: March 15, 2011Condition(s): Ventilator Time; Length of ICU Stay; Length of Hospital Stay; Pain
- 9RecruitingLast Updated: July 6, 2010Condition(s): Cystoscopy
- 10RecruitingLast 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
- 11CompletedLast Updated: October 5, 2011Condition(s): Cardiovascular Diseases
- 12RecruitingLast Updated: March 21, 2006Condition(s): Hematuria; Urination Disorders; Recurrent Urinary Tract Infection
- 13CompletedLast Updated: July 22, 2008Condition(s): Pleural Effusion; Pleural Diseases
- 14RecruitingLast Updated: April 27, 2012Condition(s): Osteoporosis
- 15RecruitingLast Updated: March 16, 2011Condition(s): Glaucoma
- 16RecruitingLast Updated: April 17, 2012Condition(s): Anesthesia
- 17CompletedLast Updated: December 13, 2010Condition(s): Airway
- 18RecruitingLast Updated: April 24, 2012Condition(s): Gallstone Disease
- 19CompletedLast Updated: March 26, 2008Condition(s): Erectile Dysfunction
- 20CompletedLast Updated: May 20, 2009Condition(s): Dental Trauma
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/?cond=%22Muscle+Rigidity%22
