muscular dystrophy
Information
- Disease name
- muscular dystrophy
- Disease ID
- DOID:9884
- Description
- "A myopathy is characterized by progressive skeletal muscle weakness degeneration." [url:http\://en.wikipedia.org/wiki/Muscular_dystrophy, url:http\://www.ninds.nih.gov/disorders/md/md.htm]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT04038138 | Active, not recruiting | N/A | Clinical Trial Readiness Network FSHD France: Prospective 24 Months MRI Study | September 16, 2019 | September 16, 2025 |
| NCT00001164 | Completed | Studies of Patients With Skin Disease, Patients With Neurological Degenerations, and Normal Volunteers | July 1978 | June 2000 | |
| NCT00622453 | Completed | Arrhythmias in Myotonic Muscular Dystrophy | September 1996 | February 2015 | |
| NCT00866112 | Completed | N/A | A Randomized Exercise Trial for Wheelchair Users | May 2008 | June 2012 |
| NCT01393444 | Completed | N/A | ECoG Direct Brain Interface for Individuals With Upper Limb Paralysis | May 2011 | April 2015 |
| NCT01451281 | Completed | Studying Skeletal Muscle, Heart, and Diaphragm Imaging in Boys With Duchenne Muscular Dystrophy | September 15, 2011 | May 20, 2019 | |
| NCT01790178 | Completed | N/A | Ultrasound in Muscle Biopsy | February 2013 | October 2015 |
| NCT01882400 | Completed | Phase 4 | Assessment of Response to Treatment of Osteoporosis With Oral Bisphosphonates in Patients With Muscular Dystrophy | May 2001 | September 2007 |
| NCT01950897 | Completed | Muscle Tissue Bank for Muscular Dystrophy | August 24, 2005 | June 9, 2015 | |
| NCT01990976 | Completed | Study of Morphology and Functional Magnetic Resonance Imaging (MRI) Muscle Patients With Muscular Dystrophy Type FSHD Benefiting a Physical Training Introduced. | May 2012 | June 2015 | |
| NCT02104921 | Completed | Innovative Ultrasound Technology in Neuromuscular Disease | December 1, 2013 | March 1, 2020 | |
| NCT02218593 | Completed | WREX Outcome Study | July 2014 | July 2015 | |
| NCT02428673 | Completed | N/A | Effects of Standing on Non-Ambulatory Children With Neuromuscular Conditions | December 9, 2015 | March 23, 2018 |
| NCT02522507 | Completed | N/A | A Peer E-mentoring Intervention to Improve Employment | January 2016 | July 2020 |
| NCT02745938 | Completed | GDF-15 as a Biomarker for Mitochondrial Disease | June 2016 | August 2017 | |
| NCT02815878 | Completed | N/A | Enhance Wellness for Individuals With Long-Term Physical Disabilities | May 12, 2014 | November 2017 |
| NCT04035967 | Completed | Investigation of Parents' Anxiety Level and Health Related Quality of Life in Different Types of Physical Disabilities | May 1, 2017 | May 1, 2019 | |
| NCT04154098 | Completed | N/A | Evaluation of a Textile Scapula Orthosis | November 1, 2019 | July 13, 2020 |
| NCT05228405 | Completed | Awareness Levels of Caregivers of Disabled Children | April 15, 2019 | August 15, 2019 | |
| NCT01459302 | Enrolling by invitation | Genetic Study of Familial and Sporadic ALS/Motor Neuron Disease, Miyoshi Myopathy and Other Neuromuscular Disorders | January 2009 | October 2024 | |
| NCT06363526 | Not yet recruiting | N/A | Effectiveness of 5-week Digital Respiratory Practice in a Group of Children With Duchenne Muscular Dystrophy and Becker Muscular Dystrophy. | May 5, 2024 | November 30, 2024 |
| NCT05715957 | Not yet recruiting | Follow-up Study on Female Carriers With DMD Gene Variants | March 1, 2023 | August 1, 2025 | |
| NCT06290713 | Not yet recruiting | Phase 2 | Vasodilator and Exercise Study for DMD (VASO-REx) | March 2024 | November 2026 |
| NCT05470478 | Not yet recruiting | N/A | iBCI Optimization for Veterans With Paralysis | September 1, 2024 | June 30, 2026 |
| NCT00138931 | Recruiting | Genetics of Cardiovascular and Neuromuscular Disease | September 1996 | January 2025 | |
| NCT00313677 | Recruiting | Clinical Trial Readiness for the Dystroglycanopathies | April 2006 | July 2026 | |
| NCT01961557 | Recruiting | N/A | Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders | July 2, 2015 | December 31, 2025 |
| NCT05230459 | Recruiting | Phase 1/Phase 2 | A Study to Evaluate the Safety of AB-1003 (Previously LION-101) in Subjects With Genetic Confirmation of LGMD2I/R9 (Part1) | March 12, 2023 | December 2028 |
| NCT05237973 | Recruiting | Investigational Use of Neuromuscular Ultrasound | April 18, 2022 | August 3, 2026 | |
| NCT02532244 | Recruiting | Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases | June 2015 | December 2025 | |
| NCT00082108 | Recruiting | Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry | September 2000 | June 2024 | |
| NCT05644522 | Recruiting | N/A | Nomad P-KAFO Study | March 1, 2024 | December 2027 |
| NCT00912041 | Recruiting | N/A | BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia | May 2009 | December 2038 |
| NCT03840928 | Recruiting | PatientSpot Formerly Known as ArthritisPower | April 1, 2015 | March 1, 2025 | |
| NCT05726591 | Recruiting | N/A | Evaluating Long-term Use of a Pediatric Robotic Exoskeleton (P.REX/Agilik) to Improve Gait in Children With Movement Disorders | May 2, 2023 | October 31, 2027 |
| NCT00004568 | Recruiting | Study of Inherited Neurological Disorders | February 18, 2000 | ||
| NCT01633242 | Terminated | Heart Imaging in Children With Muscular Dystrophy | February 24, 2012 | October 11, 2016 | |
| NCT02653833 | Terminated | Early Phase 1 | The Study of Skeletal Muscle Blood Flow in Becker Muscular Dystrophy | November 1, 2017 | September 1, 2018 |
| NCT00518817 | Unknown status | The Cardiovascular Genetic and Therapeutic Implications of Muscular Dystrophy | August 2007 | August 2009 | |
| NCT01834040 | Unknown status | Phase 1/Phase 2 | Study Safety and Efficacy of BMMNC for the Patient With Duchenne Muscular Dystrophy | September 2014 | October 2016 |
| NCT02124616 | Unknown status | National Registry for Egyptian Pediatric Neuromuscular Diseases | April 2014 | December 2020 | |
| NCT04574934 | Unknown status | N/A | Effect of Aquatic Therapy on Pulmonary Functions in Patients With Muscular Dystrophy | June 1, 2020 | October 1, 2020 |
| NCT04461561 | Unknown status | N/A | Using NPT to Evaluate Providing PPC as ELNEC-PPC WBT for Nurses | July 1, 2020 | September 1, 2021 |
| NCT01834066 | Unknown status | Phase 1/Phase 2 | Study Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Muscular Dystrophy. | September 2014 | December 2016 |
| NCT02241928 | Withdrawn | Phase 1 | Stem Cell Therapy in Muscular Dystrophy | January 2009 | May 2019 |
- Disase is a (Disease Ontology)
- DOID:423
- Cross Reference ID (Disease Ontology)
- GARD:7922
- Cross Reference ID (Disease Ontology)
- ICD10CM:G71.0
- Cross Reference ID (Disease Ontology)
- MESH:D009136
- Cross Reference ID (Disease Ontology)
- MIM:158800
- Cross Reference ID (Disease Ontology)
- MIM:159050
- Cross Reference ID (Disease Ontology)
- MIM:309930
- Cross Reference ID (Disease Ontology)
- MIM:309950
- Cross Reference ID (Disease Ontology)
- MIM:310000
- Cross Reference ID (Disease Ontology)
- MIM:310095
- Cross Reference ID (Disease Ontology)
- MIM:600416
- Cross Reference ID (Disease Ontology)
- NCI:C84910
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:155095006
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0026850
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0003560
- HPO alt_id (Human Phenotype Ontology)
- HP:0003544
- HPO alt_id (Human Phenotype Ontology)
- HP:0003806
- ICD10 class code (Insert disease from ICD10)
- G71.0
- ICD10 preferred id (Insert disease from ICD10)
- D0005514