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Muscular Dystrophy clinical trials

View clinical trials related to Muscular Dystrophy.

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NCT ID: NCT02428673 Completed - Cerebral Palsy Clinical Trials

Effects of Standing on Non-Ambulatory Children With Neuromuscular Conditions

Start date: December 9, 2015
Phase: N/A
Study type: Interventional

Children with neuromuscular disabilities and limited ambulation are at significant risk for decreased bone mineral density (BMD) and increased incidence of fracture. This is caused, in part, by low levels of load experienced by the skeleton due to a child's functional limitations. Low BMD has been shown to be predictive of fracture, and in fact, fractures usually occur without significant trauma in children with neuromuscular conditions. The discomfort and distress from fractures in this population are considerable, and the associated costs to the family and healthcare system are substantial. Numerous interventions have been devoted to improving BMD in these children. Stationary assisted standing devices are widely used and represent the standard-of-care. However, evidence supporting this approach is limited due to inadequate study designs with insufficient numbers of patients. This study will use load-sensing platforms in patients with neuromuscular conditions. Successful completion of this pilot study will assist in the development of a future multicenter clinical trial to definitively determine relationships, if any, between passive standing and measures of BMD, fracture incidence, pulmonary function, and health-related quality-of-life measures in children with a variety of neuromuscular disabilities (e.g., spinal muscular atrophy, cerebral palsy, muscular dystrophy, spina bifida, Rett syndrome). Hypothesis: Assisted standing treatment program will gradually increase their duration of standing by up to 75% after the baseline phase.

NCT ID: NCT02241928 Withdrawn - Muscular Dystrophy Clinical Trials

Stem Cell Therapy in Muscular Dystrophy

Start date: January 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study was to analyze the effect of autologous bone marrow mononuclear cells in muscular dystrophy.

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: NCT02124616 Recruiting - Clinical trials for Spinal Muscular Atrophy

National Registry for Egyptian Pediatric Neuromuscular Diseases

Start date: April 2014
Phase: N/A
Study type: Observational [Patient Registry]

Our aim is to establish multi-center national Egyptian database of information for inherited and acquired neuromuscular diseases in infants and children from 0 to 18 years of age.

NCT ID: NCT02104921 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Innovative Ultrasound Technology in Neuromuscular Disease

AQUIRe
Start date: December 1, 2013
Phase:
Study type: Observational

This study is utilizing ultrasound measurement to measure neuromuscular disease status in adult patients. The hypothesis is the by quantifying ultrasound data, it is possible that ultrasound can be utilized as a tool to determine if a disease is responding to therapy or progressing.

NCT ID: NCT01990976 Completed - Muscular Dystrophy Clinical Trials

Study of Morphology and Functional Magnetic Resonance Imaging (MRI) Muscle Patients With Muscular Dystrophy Type FSHD Benefiting a Physical Training Introduced.

FSHD3
Start date: May 2012
Phase: N/A
Study type: Observational

The safety of guided practice of physical activity in myopathies is increasingly accepted, including muscular dystrophies. In facioscapulohumeral dystrophy (FSHD), one of the most common muscular dystrophy, the aerobic training showed its physiological and functional efficiency without affecting the quality of life of patients. The issue of exercise therapy extended to all neuromuscular diseases, as has been rigorously analyzed, shows that the use of a training program combining endurance exercise targeted exercises and strength is even more relevant. To complete the multidimensional assessments be managed by each team ( physiological assessments, functional tissue and quality of life) it is relevant to continue , for a descriptive study quantitative and qualitative analyzes by muscle imaging and spectroscopy (MRI and Nuclear Resonance Imaging (NMR) spectroscopy ).

NCT ID: NCT01961557 Recruiting - Cerebral Palsy Clinical Trials

Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders

Start date: July 2, 2015
Phase: N/A
Study type: Interventional

Background: - Cerebral palsy (CP) is the most common motor disorder in children. CP often causes crouch gait, an abnormal way of walking. Knee crouch has many causes, so no single device or approach works best for everybody. This study s adjustable brace provides many types of walking assistance. Researchers will evaluate brace options to find the best solution for each participant, and whether one solution works best for the group. Objective: - To evaluate a new brace to improve crouch gait in children with CP. Eligibility: - Children 5 17 years old with CP. - Healthy volunteers 5 17 years old. Design: - All participants will be screened with medical history and physical exam. - Healthy volunteers will have 1 visit. They will do motion analysis, EMG, and EEG described below. - Participants with CP will have 6 visits. - Visit 1: <TAB>1. Motion analysis: Balls will be taped to participants skin. This helps cameras follow their movement. <TAB>2. EMG: Metal discs will be taped to participants skin. They measure electrical muscle activity. <TAB>3. Participants knee movement will be tested. <TAB>4. Participants will walk 50 meters. <TAB>5. Participants legs will be cast to make custom braces. - Visit 2: - Participants will wear their new braces and have them adjusted. - Steps 1 3 will be repeated. - EEG: Small metal discs will be placed on the participants scalp. They record brain waves. - Participants will have electrical stimulation of their knees and practice extending them. - Participants will take several walks with the braces in different settings. - Visits 3 5: participants will repeat the walking and some other steps from visit 2. - Visit 6 will repeat visit 2.

NCT ID: NCT01950897 Completed - Clinical trials for Muscular Dystrophies

Muscle Tissue Bank for Muscular Dystrophy

Start date: August 24, 2005
Phase:
Study type: Observational

This protocol proposes to establish gene expression profiles of muscular dystrophies for correct diagnosis and for development of experimental therapies for these diseases.

NCT ID: NCT01882400 Completed - Cystic Fibrosis Clinical Trials

Assessment of Response to Treatment of Osteoporosis With Oral Bisphosphonates in Patients With Muscular Dystrophy

Start date: May 2001
Phase: Phase 4
Study type: Interventional

By supplying an adequate amount of calcium and vitamin D with the addition of weekly bisphosphonate, the investigators will be able to increase bone mass and decrease the incidence of fragility fractures in these children with muscular dystrophy. The investigators think this treatment will also decrease the intensity of pain frequently present in these patients and slow the progression of scoliosis.

NCT ID: NCT01834066 Recruiting - Muscular Dystrophy Clinical Trials

Study Safety and Efficacy of Bone Marrow Derived Autologous Cells for the Treatment of Muscular Dystrophy.

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

This Study is single arm, single centre trial to check the safety and efficacy of Bone Marrow derived autologous cell(100 million per dose) for the patient with Duchenne Muscular Dystrophy.