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Muscular Dystrophies clinical trials

View clinical trials related to Muscular Dystrophies.

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NCT ID: NCT02251600 Completed - Clinical trials for Duchenne Muscular Dystrophy

A Pharmacokinetic Study of Oral Deflazacort in Children and Adolescent Subjects With Duchenne Muscular Dystrophy

Start date: December 2014
Phase: Phase 1
Study type: Interventional

Study to characterize the single-state and steady-state dosing of oral deflazacort in pediatric and adolescents subjects.

NCT ID: NCT02246478 Completed - Clinical trials for Duchenne Muscular Dystrophy

A Study of TAS-205 for Duchenne Muscular Dystrophy

Start date: September 2014
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate the safety and pharmacokinetic of TAS-205 in patients with Duchenne Muscular Dystrophy.

NCT ID: NCT02239224 Completed - Clinical trials for Facioscapulohumeral Muscular Dystrophy (FSHD)

Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Participants With Muscular Dystrophy

Start date: September 4, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and tolerability profile of ATYR1940 in the treatment of adult participants with molecularly defined genetic muscular dystrophies

NCT ID: NCT02235844 Completed - Clinical trials for Duchenne's Muscular Dystrophy

Allogeneic Human Umbilical Cord Mesenchymal Stem Cells for a Single Male Patient With Duchenne Muscular Dystrophy (DMD)

Start date: September 2014
Phase: Phase 1
Study type: Interventional

This research study is designed to evaluate the effects of human umbilical cord mesenchymal stem cells (UC-MSCs), on Duchenne's muscular dystrophy (DMD). The potential muscle regenerative and anti-inflammatory properties of UC MSCs position them as a possible treatment option for DMD. Both of these properties could lead to potential benefits for a DMD patient.

NCT ID: NCT02218593 Completed - Clinical trials for Spinal Muscular Atrophy

WREX Outcome Study

Start date: July 2014
Phase:
Study type: Observational

This study is to evaluate how the Wilmington Robotic Exoskeleton (WREX) is working for children who are using the WREX, or have used it in the past. The survey consists of a set of questions a) performed online and b) performed over the phone.

NCT ID: NCT02207283 Completed - Clinical trials for Becker Muscular Dystrophy

PDE5 Inhibition to Alleviate Functional Muscle Ischemia in Becker Muscular Dystrophy

Start date: March 2012
Phase: Phase 4
Study type: Interventional

This study is intended to build on recent findings from our laboratory showing that a single dose of tadalafil (also known as Cialis) restored normal blood flow regulation in men with Becker muscular dystrophy. The investigators now wish to extend these findings by showing that the same dose of tadalafil will also prevent muscle injury and fatigue. Patients will take a single dose of tadalafil prior to exercising. Then doctors will measure whether the patients muscles receive more blood flow and are better protected during exercise.

NCT ID: NCT02195999 Completed - Clinical trials for Muscular Dystrophy, Duchenne

Assessment of Cardiopulmonary Function in Duchenne Muscular Dystrophy

CPI
Start date: December 2013
Phase:
Study type: Observational

This study seeks to develop and validate non-invasive assessments of cardiac and respiratory muscles with magnetic resonance imaging (MRI) to better predict the natural disease progression of Duchenne muscular dystrophy (DMD) in affected individuals over time, as well as determine whether peripheral skeletal muscle dysfunction can predict cardiopulmonary dysfunction. The central hypothesis is that non-invasive MRI measures of the heart, muscle, and peripheral skeletal muscles can sensitively predict future cardiopulmonary decline.

NCT ID: NCT02194725 Completed - Stress Clinical Trials

Where Does Hope Fit In? The Relationship Between Hope, Uncertainty, and Coping Efficacy in Mothers of Children With Duchenne/Becker Muscular Dystrophy

Start date: July 6, 2014
Phase:
Study type: Observational

Background: - Children with Duchenne/Becker Muscular Dystrophy (DBMD) slowly lose muscle function. They usually die at a young age. Some mothers adapt to the demands of caring for a child with this disease better than others. Studies show that a person s hope may positively affect how they cope and adapt. Researchers want to find out more about this. They want to develop ways to improve caregivers overall wellness. Objective: - To study the relationships between uncertainty, hope, and coping ability in mothers of children with DBMD. Eligibility: - Women in the United States 18 years and older. They must be biological mothers of a living child with DBMD and be able to answer a survey in English. Design: - This study is part of a larger study that examines the well-being of mothers with sons who have DBMD. - Participants will take a questionnaire. The questionnaire can be done on paper or on a computer. It will take 30 45 minutes to complete. - The questionnaire will include basic demographic questions about the participant and the child. There will also be questions about how the participant copes with the stress and uncertainty of DBMD. - For most of the questions, participants will rate their feelings on a scale. There will also be four open-ended questions.

NCT ID: NCT02168114 Completed - Clinical trials for Duchenne Muscular Dystrophy

Magnetic Resonance and Optical Imaging of Dystrophic and Damaged Muscle

Start date: July 2014
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine the potential of Optical Imaging techniques to detect muscle damage in boys with Duchenne Muscular Dystrophy and unaffected exercised muscle. Healthy subjects will undergo two different exercises in opposite forearms before any imaging techniques are performed. Boys with Duchenne Muscular Dystrophy will only undergo the imaging techniques without exercise.

NCT ID: NCT02167217 Completed - Clinical trials for Duchenne Muscular Dystrophy

Historically Controlled Trial of Corticosteroids in Young Boys With Duchenne Muscular Dystrophy

Start date: April 17, 2014
Phase: Phase 2
Study type: Interventional

While it has been known for many years that corticosteroid use benefits boys with Duchenne Muscular dystrophy (DMD), most clinicians do not consider treating until after age 3 or 4 years of age. The primary reason for the delay is that daily corticosteroid use has many side effects including short stature, obesity, and osteoporosis. A recent randomized blinded study of weekend oral corticosteroid use over one year showed equal improvement in strength with fewer side effects, particularly as related to growth and cushingoid changes. The investigators will test the efficacy of oral weekend corticosteroid use in infants and young boys with DMD who are under age 30 months. The investigators have demonstrated that the Bayley-III Scales of Infant development shows that infants and young boys in this age group who are untreated decline in abilities when compared to their peers. Here, in this Phase 2 historically controlled trial, the investigators will use these two measures and treat boys at five Muscular Dystrophy Association-DMD centers