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Muscular Dystrophies clinical trials

View clinical trials related to Muscular Dystrophies.

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NCT ID: NCT01851447 Active, not recruiting - Genetic Disorder Clinical Trials

Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy

Start date: November 3, 2014
Phase:
Study type: Observational

Background: - Some kinds of muscular dystrophy affect the skeletal muscle membrane. In these conditions, the muscle membrane is more fragile. This affects how the muscles contract and relax, which causes movement problems. Researchers are looking at several muscle enzymes, or chemicals that affect how muscle cells function. By studying changes in these enzymes, they may be able to better understand how muscular dystrophy affects the cells. Researchers want to collect biomarkers (chemicals from blood samples) from people with fragile sarcolemmal muscular dystrophy. This information may provide better treatments for this condition. Objectives: - To study biomarkers that may affect the muscles of people with fragile sarcolemmal muscular dystrophy. Eligibility: - Individuals at least 18 years of age with fragile sarcolemmal muscular dystrophy. Design: - Participants will be screened with a medical history and physical exam. - Participants will be asked to come for four visits to the National Institutes of Health Clinical Center. The visits will be at least 2 months apart. Each visit will require participants to stay for 5 days at the clinical center. - During each visit, participants will provide frequent small blood samples. These samples will be collected while at rest and after physical exercise. - Participants will also have a physical therapy assessment. They will perform standard motor function tests and imaging tests (MRI, MRS). These tests may take up to 1 hour each time. - Treatment will not be provided as part of this study.

NCT ID: NCT01772043 Active, not recruiting - Clinical trials for Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy Tissue Bank for Exon Skipping

Start date: September 2012
Phase: N/A
Study type: Observational

We will utilize the Cooperative International Neuromuscular Research Group (CINRG) network to collect and store tissue and blood from patients with Duchenne muscular dystrophy (DMD) with specific genetic mutations within the dystrophin gene that could be treated by antisense oligonucleotide (AO) drugs.

NCT ID: NCT01671865 Active, not recruiting - Clinical trials for Facioscapulohumeral Muscular Dystrophy

Magnetic Resonance Imaging and Spectroscopy Biomarkers for Facioscapulohumeral Muscular Dystrophy

Start date: March 2012
Phase:
Study type: Observational

The purpose of this research study is to identify and study changes in muscle in people with facioscapulohumeral muscular dystrophy using magnetic resonance imaging and spectroscopy.

NCT ID: NCT01633866 Active, not recruiting - Clinical trials for Duchenne Muscular Dystrophy

Pediatric Radio Frequency Coils Generic

Start date: July 2012
Phase:
Study type: Observational

The purpose of this study is to evaluate and optimize advances in radio frequency (RF) coil magnetic resonance imaging (MRI) technology at Cincinnati Children's Hospital Medical Center (CCHMC).

NCT ID: NCT01539772 Active, not recruiting - Clinical trials for Becker Muscular Dystrophy

Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping

Start date: April 2012
Phase:
Study type: Observational

This is a multi-center natural history study that will be conducted at participating centers in the Cooperative International Neuromuscular Research Group (CINRG). Following a baseline evaluation, participants will have three follow-up visits over a three-year period. The investigators will characterize the Becker muscular dystrophy phenotype, and correlate specific abnormal dystrophin proteins with the range of clinical outcomes.

NCT ID: NCT01521546 Active, not recruiting - Clinical trials for Duchenne Muscular Dystrophy

Eplerenone for Subclinical Cardiomyopathy in Duchenne Muscular Dystrophy

E-SCAR DMD
Start date: February 2012
Phase: N/A
Study type: Interventional

Duchenne muscular dystrophy (DMD), the most common muscular dystrophy, leads to skeletal and cardiac muscle damage. Treatment of pulmonary complications has improved survival; however, heart muscle disease or cardiomyopathy has emerged as a leading cause of death, typically by the third decade. Although myocardial changes begin early, clinically significant heart disease is rarely detected in the first decade of life. Consequently, DMD cardiomyopathy frequently goes unrecognized (and untreated) until advanced (and irreversible). Current DMD cardiovascular care guidelines recommend beta-blockers and angiotensin converting enzyme inhibitors (ACEIs) when decreased ejection fraction (EF) is noted by echocardiography (echo); however, this strategy has not significantly improved outcomes. Our team has recently made a breakthrough in a mouse study, showing in a model that causes the same heart muscle disease in humans with DMD adding an old medicine traditionally used for high blood pressure and late-stage heart failure can actually prevent heart muscle damage. Because of this drug's proven safety in both children and adults, it is ready to be studied immediately in an RCT in patients with DMD to hopefully show, as we did in mice, that we can prevent the devastating consequences of heart muscle damage.

NCT ID: NCT00674843 Active, not recruiting - Clinical trials for Muscular Dystrophies

The Efficacy of Using Far Infrared Radiation to Manage Muscular Dystrophies

Start date: May 2008
Phase: Phase 1
Study type: Interventional

The muscular dystrophies (MD) are a group of more than 30 neuromuscular disorders that are characterized by progressive skeletal muscle weakness, defects in muscle proteins and the death of muscle cells and tissue. This study will investigate the use of far infrared radiation for managing muscular dystrophies.

NCT ID: NCT00468832 Active, not recruiting - Clinical trials for Duchenne Muscular Dystrophy

Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD)

Start date: December 2005
Phase: N/A
Study type: Observational

The purpose of this study is to establish the largest long-term assessment of people with Duchenne muscular dystrophy (DMD). In this study, the investigators associated with the Cooperative International Neuromuscular Research Group CINRG) will take a detailed look (for a minimum of eight years) at DMD participant's physical abilities, the medical problems they experience, and how they use health care services. Physical abilities will be compared to a group of healthy controls. The second purpose of this study is to find out whether small, normal differences in the genetic makeup of people with DMD (called "single nucleotide polymorphisms" or "SNPs") affect how their disease progresses and relates to muscle strength/size and steroid response. The third purpose of this study is to study genetic variations associated with DMD. The final purpose of this study is to determine whether certain biomarkers are present in people with DMD and not in healthy controls.