myopathy
Information
- Disease name
- myopathy
- Disease ID
- DOID:423
- Description
- "A muscular disease in which the muscle fibers do not function resulting in muscular weakness." [url:http\://en.wikipedia.org/wiki/Myopathy]
Disease area statistics
Chromosome band
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00937001 | Active, not recruiting | N/A | Critical Illness Myopathy as a Cause of Debilitating ICU-Acquired Weakness | November 2008 | December 2025 |
NCT04881214 | Active, not recruiting | N/A | COVID-19 Pneumonia: Pulmonary Physiology, Health-related Quality of Life and Benefit of a Rehabilitation Program | July 1, 2020 | June 30, 2023 |
NCT03751644 | Completed | N/A | Peripherical Neuromuscular Electrical Stimulation in Systemic Autoimmune Myopathies | November 1, 2018 | April 29, 2021 |
NCT03141749 | Completed | Venous Thromboembolism in DM1 | January 2000 | January 2017 | |
NCT02765828 | Completed | Identification of Tongue Involvement in Late-Onset Pompe Disease | May 25, 2016 | July 15, 2019 | |
NCT01047163 | Completed | Maintenance of Muscle Mass in Older People: the Negative Impact of Statin Therapy | June 2009 | December 2012 | |
NCT02706314 | Completed | Impact of Human Blood Serum From Critically Ill Patients on Human Colon Neuronal Networks. | March 2016 | April 16, 2019 | |
NCT00120055 | Completed | Phase 4 | Association Between Systemic Exposure of Atorvastatin and Metabolites and Atorvastatin-induced Myotoxicity | February 2005 | April 2005 |
NCT02442986 | Completed | Neurological Outcome in Surgical and Non-surgical Septic Patients | November 2012 | March 2017 | |
NCT01530841 | Completed | N/A | Efficacy and Tolerance of AVAPS Mode in Myotonic Dystrophy | July 2012 | May 2016 |
NCT01547767 | Completed | Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy | February 1, 2012 | March 3, 2021 | |
NCT01642056 | Completed | Phase 1/Phase 2 | EPI-743 for Metabolism or Mitochondrial Disorders | September 1, 2012 | September 24, 2019 |
NCT01702987 | Completed | N/A | Evaluation of Ubiquinol on Mitochondrial Oxidative Capacity in Statin Patients Using 31PMRS | October 2012 | October 2013 |
NCT02011282 | Completed | N/A | Electro-Neuro-Muscular Stimulation in ICU | October 2013 | March 2015 |
NCT01790178 | Completed | N/A | Ultrasound in Muscle Biopsy | February 2013 | October 2015 |
NCT02104921 | Completed | Innovative Ultrasound Technology in Neuromuscular Disease | December 1, 2013 | March 1, 2020 | |
NCT06374719 | Recruiting | WiTNNess - TNNT1 Myopathy Natural History Study | September 23, 2018 | June 1, 2027 | |
NCT01353430 | Recruiting | Characterization of Inclusion Body Myopathy Associated With Paget's Disease of Bone and Frontotemporal Dementia (IBMPFD) | November 15, 2007 | December 2026 | |
NCT03660969 | Recruiting | Reliability of Cardiac Troponins for the Diagnosis of Myocardial Infarction in the Presence of Skeletal Muscle Disease | January 1, 2018 | January 1, 2027 | |
NCT03749538 | Recruiting | N/A | Acute Transcranial Direct Current Stimulation in Patients With Systemic Autoimmune Myopathies | October 1, 2018 | May 7, 2024 |
NCT03998540 | Recruiting | Improvement of DIAgnostic and Phenotype-genotype Correlation Studies in Patients With MYOpathy Suspected of TITinopathy | December 5, 2019 | May 5, 2025 | |
NCT04678635 | Recruiting | N/A | Chronic Transcranial Direct Current Stimulation in Patients With Systemic Autoimmune Myopathies | December 12, 2020 | May 7, 2024 |
NCT05599568 | Recruiting | N/A | Repeated Bout Effect i Neuromuscular Diseases | May 15, 2022 | May 30, 2025 |
NCT00278564 | Terminated | Phase 1 | Stem Cell Transplantation in Idiopathic Inflammatory Myopathy Diseases | September 2005 | July 2016 |
NCT02247895 | Terminated | N/A | Treatment of Muscle Weakness in Critically Ill Patients | December 2016 | February 2018 |
NCT03633565 | Unknown status | Phase 4 | Comparative Study of Strategies for Management of Duchenne Myopathy (DM) | September 2018 | November 2021 |
NCT00549029 | Unknown status | The Association of Genetic Polymorphisms With Statin-Induced Myopathy. | August 2007 | January 2008 | |
NCT00767130 | Unknown status | DNA Diagnostic System for Statin Safety and Efficacy | January 2007 | December 2009 | |
NCT04941079 | Unknown status | Safety and Efficacy of Inactivated SARS-CoV-2 Vaccine in Immune-related Myopathy (Myasthenia Gravis and Inflammatory Myopathy) Patients :a Prospective Observational Study | June 30, 2021 | December 31, 2021 | |
NCT01225614 | Unknown status | Phase 3 | Efficacy and Tolerance of Early Launching of Nocturnal Non Invasive | October 2010 | December 2018 |
NCT03042286 | Unknown status | SAPhIRE Statin Adverse Drug Reaction | March 2015 | January 2020 | |
NCT02235220 | Unknown status | N/A | Reduction of Masticatory Muscle Activity by Restoring Canine Guidance | September 2014 | December 2015 |
NCT01022450 | Unknown status | Study of the Causes of the Breakdown of Muscle Fibers in Hospitalized Patients | November 2009 | ||
NCT00990834 | Withdrawn | N/A | Muscle Characteristics Associated With Statin Therapy | November 2009 | June 2011 |
NCT02124070 | Withdrawn | Phase 1/Phase 2 | Therapeutic Effect of Recombinant Human Growth Hormone (rhGH) on the Myopathy of Cystinosis | March 26, 2014 | November 6, 2015 |
NCT01395563 | Withdrawn | N/A | Strength Training on Pancreatic Cancer | January 2009 | December 2011 |
- Disase is a (Disease Ontology)
- DOID:66
- Cross Reference ID (Disease Ontology)
- ICD10CM:G72.9
- Cross Reference ID (Disease Ontology)
- ICD9CM:359.9
- Cross Reference ID (Disease Ontology)
- MESH:D009135
- Cross Reference ID (Disease Ontology)
- NCI:C101216
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:155094005
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0026848
- HPO alt_id (Human Phenotype Ontology)
- HP:0003569
- HPO alt_id (Human Phenotype Ontology)
- HP:0003705
- HPO alt_id (Human Phenotype Ontology)
- HP:0003742
- HPO alt_id (Human Phenotype Ontology)
- HP:0003802
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0003198