Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting
368 studies found for:    Muscular Dystrophy
Show Display Options
Rank Status Study
1 Completed Evaluation of Limb-Girdle Muscular Dystrophy
Conditions: Becker Muscular Dystrophy;   Limb-Girdle Muscular Dystrophy, Type 2A (Calpain-3 Deficiency);   Limb-Girdle Muscular Dystrophy, Type 2B (Miyoshi Myopathy, Dysferlin Deficiency);   Limb-Girdle Muscular Dystrophy, Type 2I (FKRP-deficiency)
2 Recruiting Double Push Acoustic Radiation Force (DP ARF) Ultrasound for Monitoring Degeneration in Duchenne Muscular Dystrophy
Condition: Muscular Dystrophy, Duchenne
3 Unknown  The Efficacy of Using Far Infrared Radiation to Manage Muscular Dystrophies
Condition: Muscular Dystrophies
Intervention: Radiation: Far Infrared Radiation
4 Unknown  Study Safety and Efficacy of BMMNC for the Patient With Duchenne Muscular Dystrophy
Conditions: Muscular Dystrophy;   Duchenne Muscular Dystrophy
Intervention: Other: Intralesional/ Intravenous of Autologous Stem cells.
5 Recruiting Efficacy Safety of Granulocyte Colony-stimulating Factor Treatment Children and Adolescents With Muscular Dystrophy
Condition: Increase of Muscle Strength in Patients With Muscular Dystrophy
Intervention: Drug: Granulocyte colony-stimulating factor (Filgrastim)
6 Active, not recruiting Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Patients With Muscular Dystrophy
Condition: Facioscapulohumeral Muscular Dystrophy (FSHD)
Intervention: Biological: ATYR1940
7 Terminated Heart Imaging in Children With Muscular Dystrophy
Condition: Muscular Dystrophy
8 Unknown  Muscle MRI in Becker Muscular Dystrophy and in Limb-girdle Muscular Dystrophy Type 2I
Conditions: Becker Muscular Dystrophy;   Limb-Girdle Muscular Dystrophy Type 2I
9 Recruiting Pilot Study of Cardiac MR in Patients With Muscular Dystrophy
Conditions: Muscular Dystrophies;   Cardiac Fibrosis;   Genetic Diseases, Inborn;   Musculoskeletal Diseases
10 Unknown  Establishment of Phenotypic Profiles of Muscular Dystrophies for Understanding Disease Progression, Diagnosis and Development of New Therapies
Conditions: Muscular Dystrophies;   Muscular Dystrophy
11 Active, not recruiting Efficacy of Stem Cell Therapy in Ambulatory and Non-ambulatory Children With Duchenne Muscular Dystrophy - Phase 1-2
Condition: Duchenne Muscular Dystrophy
Intervention: Drug: Biological: Umbilical Cord Based Allogenic Mesenchymal Stem Cell
12 Active, not recruiting Arrhythmias in Myotonic Muscular Dystrophy
Conditions: Muscular Dystrophy;   Arrhythmia;   Sudden Cardiac Death
Intervention: Other: Screening
13 Recruiting Limb Girdle Muscular Dystrophy (LGMD) Natural History
Condition: Muscular Dystrophies, Limb-Girdle (GENETICALLY CONFIRMED)
14 Completed Gentamicin Treatment of Muscular Dystrophy
Conditions: Becker Muscular Dystrophy;   Duchenne Muscular Dystrophy
Intervention: Drug: Gentamicin
15 Enrolling by invitation Clinical Trial of Coenzyme Q10 and Lisinopril in Muscular Dystrophies
Conditions: Duchenne Muscular Dystrophy;   Becker Muscular Dystrophy;   Limb Girdle Muscular Dystrophy
Intervention: Drug: Coenzyme Q10 and Lisinopril
16 Recruiting The Study of Skeletal Muscle Blood Flow in Becker Muscular Dystrophy
Condition: Muscular Dystrophy
Intervention: Drug: Ranolazine
17 Recruiting DuchenneConnect Registry
Conditions: Duchenne Muscular Dystrophy;   Becker Muscular Dystrophy
18 Completed Cardiac Outcome Measures in Children With Muscular Dystrophy
Conditions: Duchenne Muscular Dystrophy;   Becker Muscular Dystrophy;   Limb Girdle Muscular Dystrophy
19 Recruiting Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry
Conditions: Myotonic Dystrophy;   Facioscapulohumeral Muscular Dystrophy;   Muscular Dystrophy;   Myotonic Dystrophy Type 1;   Myotonic Dystrophy Type 2;   Congenital Myotonic Dystrophy;   PROMM (Proximal Myotonic Myopathy);   Steinert's Disease;   Myotonic Muscular Dystrophy
20 Completed Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)
Condition: Muscular Dystrophies
Interventions: Genetic: rAAV1.tMCK.human-alpha-sarcoglycan- First cohort;   Genetic: Genetic: rAAV1.tMCK.human-alpha-sarcoglycan- Second cohort

   Previous Page Studies Shown (1-20) Next Page (21-40) Show next page of results    Last Page
Indicates status has not been verified in more than two years