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Myotonic Dystrophy clinical trials

View clinical trials related to Myotonic Dystrophy.

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NCT ID: NCT01406873 Completed - Myotonic Dystrophy Clinical Trials

Clinical Efficacy Trial of Mexiletine for Myotonic Dystrophy Type 1

Start date: June 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effects of mexiletine treatment for 6 months on ambulation, myotonia, muscle function and strength, pain, gastrointestinal functioning, cardiac conduction, and quality of life in myotonic dystrophy type 1 (DM1).

NCT ID: NCT01242007 Completed - Myotonic Dystrophy Clinical Trials

Postural Spirometry Changes in Ambulatory Myotonic Dystrophy Patients

Start date: April 2008
Phase: N/A
Study type: Interventional

Myotonic dystrophy Type 1 (MD1, Steinert's disease), an autosomal dominant multisystem disease, is of the most common muscular dystrophies in adults, with a European prevalence of 3-15/100 000. The disease course is progressive, associating muscular weakness, wasting and myotonia. Respiratory dysfunction is common, involving a restrictive ventilatory abnormality and alveolar hypoventilation, originating from respiratory muscle weakness. Depending on the degree of impairment of their lung function, the quality of life and the prognosis of MD1 patients may be very variable. However, time course and prevalence of such respiratory function impairment have not been clearly identified. More importantly, factors able to predict poor respiratory outcome have not been defined and therefore early prognosis can not be assessed during the follow-up of these patients. In other neuromuscular disorders, especially Amyotrophic Lateral Sclerosis (ALS), postural spirometry has been recommended to improve the detection of diaphragmatic involvement and some authors have suggested that the supine fall in the forced vital capacity could be used to initiate noninvasive positive pressure ventilation and predicts some respiratory symptoms. In a sample of ambulatory patients with MD1, our study was designed to prospectively achieve two aims: 1) to assess the respective prevalence of a ventilatory restrictive pattern, respiratory muscle weakness, hypoxemia and hypercapnia and 2) to evaluate whether postural changes in lung volumes contribute to sensitize the diagnosis of respiratory weakness and could be used as a predictor of poor respiratory function, including hypoxemia, hypercapnia and restrictive ventilatory disease.

NCT ID: NCT01136330 Completed - Myotonic Dystrophy Clinical Trials

DM1 Heart Registry - DM1 Respiratory Registry

DM1-Heart-R
Start date: May 2010
Phase: N/A
Study type: Observational

Myotonic dystrophy type 1 (DM1) is the most frequent neuromuscular disease in adults. DM1 patients have an impaired prognosis (mean age of death <60 years) due to cardiac and respiratory complications. Our primary objective was to identify cardiac and respiratory prognostic factors in DM1.

NCT ID: NCT00622453 Completed - Arrhythmia Clinical Trials

Arrhythmias in Myotonic Muscular Dystrophy

DM1
Start date: September 1996
Phase: N/A
Study type: Observational

Adult myotonic muscular dystrophy (Steinert's disease) is the most common inherited neuromuscular disorder. Cardiac rhythm disturbances occur frequently in this disease state and may be responsible for up to one-third of deaths. In this study, we intend to evaluate the utility of non-invasive electrocardiographic screening methods and history in predicting serious arrhythmic events.

NCT ID: NCT00577577 Completed - Clinical trials for Myotonic Dystrophy Type 1

Safety and Efficacy Study of Recombinant Human Insulin-Like Growth Factor-I/Recombinant Human Insulin-Like Growth Factor Binding Protein-3 (rhIGF-I/rhIGFBP-3) In Myotonic Dystrophy Type 1

Start date: December 2007
Phase: Phase 2
Study type: Interventional

To investigate the effects of rhIGF-I/rhIGFBP-3 treatment for 24 weeks on endurance, ambulation, cognitive functioning, insulin resistance, lipid levels, muscle function and strength, pain, gastrointestinal functioning, and quality of life endpoints in DM1 patients

NCT ID: NCT00233519 Completed - Myotonic Dystrophy Clinical Trials

Effects of SomatoKine (Iplex)Recombinant Human Insulin-like Growth Factor-1/Recombinant Human Insulin-like Growth Factor-binding Protein-3 (rhIGF-I/rhIGFBP-3) in Myotonic Dystrophy Type 1 (DM1)

Start date: November 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to investigate the safety and feasibility of daily subcutaneous injections of recombinant IGF1 complexed with IGF binding protein 3 (SomatoKine-INSMED) as a treatment for muscle wasting and weakness in myotonic dystrophy type 1.

NCT ID: NCT00167609 Completed - Myotonic Dystrophy Clinical Trials

Efficacy and Safety of DHEA for Myotonic Dystrophy

Start date: November 2004
Phase: Phase 2/Phase 3
Study type: Interventional

To test the efficacy and safety of two doses of dehydroepiandrosterone (DHEA) in adults with myotonic dystrophy

NCT ID: NCT00004769 Completed - Clinical trials for Myotonic Muscular Dystrophy

Study of Muscle Wasting and Altered Metabolism in Patients With Myotonic Dystrophy

Start date: December 1993
Phase: N/A
Study type: Observational

OBJECTIVES: I. Examine the interrelationships between muscle wasting (phenotype), the degree of myotonic dystrophy (DM) gene expression (genotype) in patients with DM. II. Characterize the insulin resistance in these patients. III. Assess the glucose uptake in the leg and forearm tissues of these patients. IV. Determine the stability of the DM gene lesion in muscles over a 5-10 year period.