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Muscular Diseases clinical trials

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NCT ID: NCT03547687 Completed - Clinical trials for Intensive Care (ICU) Myopathy

Neurosciences-Intensive Care Unit Electrical Stimulation

Start date: August 10, 2018
Phase: N/A
Study type: Interventional

Patients admitted to the Neurosciences Intensive Care Unit (NSICU) are at particular risk of developing ICU-associated weakness and myopathy, given the unique risks of early mobilization in these patients, which include increased intracranial pressure, hemodynamic instability, vasospasm, decreased cerebral blood flow with resultant cerebral ischemia, and delirium. Interventions that could provide some of the benefits of early mobilization without these risks would be of great utility in the NSICU. A number of studies have demonstrated that electrical stimulation of the lower extremity muscles, generally the quadriceps, can retard disuse atrophy and loss of strength associated with medical ICU stays, and one study has shown reduced length of intubation and accelerated functional recovery. This pilot trial will evaluate the impact of electrical stimulation on patients in the NSICU, with a hypothesis that electrical stimulation treatments will reduce the length of hospital stay and intubation and improve functional recovery. In this trial, intubated patients admitted to the NSICU will have electrical stimulation applied to the quadriceps muscle groups on both lower extremities simultaneously for 45 minutes at a time for a total of 5 treatments each week, for up to 14 days or until ICU discharge, whichever comes first.

NCT ID: NCT03531554 Completed - VLCAD Deficiency Clinical Trials

Acute Nutritional Ketosis in VLCAD Deficiency

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

To test if a ketone-ester based drink can boost muscle mitochondrial function in vivo in patients with VLCADD in order to establish a rational basis for therapeutic use in this disorder.

NCT ID: NCT03513835 Completed - Healthy Controls Clinical Trials

Diagnostic Screening Tests and Potential Biomarkers in Mitochondrial Myopathies

Start date: January 1, 2018
Phase:
Study type: Observational

The purpose of this study is to develop simple diagnostic screeningtests and investigate potential biomarkers for identifying patients with abnormalities of mitochondrial function, which also can be used as outcome measures in future clinical trials. The study will investigate two submaximal tests: a submaximal handgrip test and a walking test. Furthermore investigators will investigate Acyl-carnitine profiles and GDF-15 levels in patients with mitochondrial myopathy.

NCT ID: NCT03440034 Completed - Clinical trials for Nervous System Diseases

Study of Pioglitazone in Sporadic Inclusion Body Myositis

Start date: May 22, 2018
Phase: Phase 1
Study type: Interventional

A study looking at the effect of pioglitazone in skeletal muscle of patients with sporadic inclusion body myositis (sIBM).

NCT ID: NCT03406780 Completed - Clinical trials for Nervous System Diseases

A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy

HOPE-2
Start date: March 4, 2018
Phase: Phase 2
Study type: Interventional

HOPE-2 is a double-blind clinical trial evaluating the safety and efficacy of a cell therapy called CAP-1002 in study participants with Duchenne muscular dystrophy (DMD). Non-ambulatory and ambulatory boys and young men who meet eligibility criteria will be randomly assigned to receive either CAP-1002 or placebo every 3 months for a total of 4 doses during a 12-month period.

NCT ID: NCT03384420 Completed - Clinical trials for Mitochondrial Diseases

A Study to Evaluate the Safety and Therapeutic Effects of Transplantation of MNV-BM-BLD in Pediatric Patients With Pearson Syndrome

Start date: February 13, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Mitochondrial diseases are a genetically heterogeneous group of disorders caused by mutations or deletions in mitochondrial DNA (mtDNA) displaying a wide range of severity and phenotypes. These diseases may be inherited from the mother (mitochondrial inheritance) or non-inherited. The latter are ultra-rare pediatric diseases caused by a mutation or deletion of mtDNA, which develop into a systemic multi organ disease and eventually death. MNV-BM-BLD is a therapeutic process for enrichment of patient's peripheral hematopoietic stem cells with normal and healthy mitochondria derived from donor blood cells. The process, called mitochondria augmentation therapy, aims to reduce the symptoms of mitochondrial diseases.

NCT ID: NCT03354767 Completed - Muscular Diseases Clinical Trials

The Role of Ischaemia-reperfusion Injury in the Pathogenesis of Muscle Wasting After Thoracic Aortic Surgery

RIMMAS
Start date: November 2013
Phase: N/A
Study type: Observational

Single-centre observational study over one year investigating the mechanisms of muscle homeostasis in patients with acute skeletal muscle atrophy following major aortic surgery

NCT ID: NCT03351270 Completed - Clinical trials for Centronuclear Myopathy

Prospective Natural History Study of Patients With Myotubular Myopathy and Other CentroNuclear Myopathies

NatHis-CNM
Start date: May 28, 2017
Phase: N/A
Study type: Interventional

This is the 2 years extension of the prospective and longitudinal study of the natural history and functional status of patients with myotubular myopathy and other centronuclear (CNM) sponsored by Dynacure including ten additional pediatric patients with mutation in MTM1 or DNM2 genes). the patients are planned to be enrolled in one year leading to an expected total number of 70 patients followed at least over 1 year period. Data from the study will be used to characterize the disease course of CNM and determine which outcome measures will be the best to assess the efficacy of potential therapies.

NCT ID: NCT03268421 Completed - Fibromyalgia Clinical Trials

Fibromyalgia Integrative Training for Adolescents With Juvenile Fibromyalgia

FIT Teens
Start date: January 2, 2018
Phase: N/A
Study type: Interventional

This study evaluates whether Fibromyalgia Integrative Training program for Teens (FIT Teens), a combined cognitive behavioral therapy and neuromuscular exercise training program is more effective in reducing disability in adolescents with Juvenile Fibromyalgia compared to cognitive behavioral therapy (CBT) alone or a graded aerobic exercise (GAE) program alone. One third of participants will receive the FIT Teens training; one third will receive CBT training; and one third of participants will receive the GAE training.

NCT ID: NCT03267277 Completed - Dermatomyositis Clinical Trials

Sodium Thiosulfate for Treatment of Calcinosis Associated With Juvenile and Adult Dermatomyositis

Start date: October 5, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Dermatomyositis (DM) and juvenile dermatomyositis (JDM) cause inflammation in the muscles. People with DM and JDM can develop calcium deposits in places they should not, known as calcinosis. Calcinosis can be painful and cause disabilities and other problems. Researchers want to learn more about calcinosis to find treatments for it. Objective: To test if sodium thiosulfate (STS) can treat people with DM with calcinosis. Eligibility: People ages 7 and older who have moderate or severe calcinosis. They must have stable DM and calcium deposits in the torso or at least 2 limbs. Design: Participants will be screened with: - Medical history - Physical exam - Muscle strength and function tests - Blood and urine tests Participants will have several visits: - 7-day pre-treatment visit about 10 weeks before starting STS - Treatment visits over 10 weeks. They will get STS 3 times a week through IV infusion. They may be hospitalized the whole time. If they tolerate the drug, they may be discharged at certain times. During these times, they will return for the infusions. - 3- to 5-day post-treatment visits 24 weeks and 62 weeks after starting STS. Visits may include repeats of screening tests and: - Questionnaires - Scans: They lie in a machine that takes pictures of the body. They may be injected with a radioactive agent. - Durometry: A small instrument applies pressure on the skin or exposed calcinosis. - Measurements of blood flow in the arms and fingernail blood vessels - Photographs of the skin - Kidney ultrasound - Tests of kidney function - Calcinosis aspiration: A needle placed into areas of calcinosis removes liquid.