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Neuromuscular Diseases clinical trials

View clinical trials related to Neuromuscular Diseases.

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NCT ID: NCT01644162 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Ventilator Monitoring in Early Exacerbation Detection

Start date: July 2012
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether respiratory disease exacerbations (a sudden worsening of symptoms) can be predicted by variables that are monitored by non-invasive ventilators (small machines that assist breathing) in patients requiring long term home ventilation. The investigators hypothesise that acute exacerbations of patients with respiratory disease and ventilatory failure will be predicted by changes in the respiratory variables monitored and stored by ventilators during chronic home ventilator use.

NCT ID: NCT01621984 Completed - Clinical trials for Neuromuscular Disease

Therapeutic Riding and Neuromuscular Disease

TR NMD
Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this current prospective study is to assess the effects of a Therapeutic Riding exercise program conducted in patients suffering from neuromuscular disease. The exercise intervention aims at improving gross motor function, gross motor performance, balance, spasticity, posture and quality of life. Patients were randomized according to age, sex, mental ability and gross motor function. Furthermore, patients will be subdivided into categories of central nervous system (brain/ spinal cord) and peripheral (peripheral nerve or muscle) diseases. The exercise program duration will be 12 weeks, once a week with 30-40 minutes sessions. Six measurements will be conducted: the Gross Motor Function Measure, the Gross Motor Performance Measure, the Quality of life Questionnaire for Children, the Pediatric Balance Scale, the dynamic plate in combination with x-ray for posture control, the Modified Ashworth Scale for spasticity and the Wisc 3 for mental ability. The results will be collected and evaluated using the statistical programme SPSS.

NCT ID: NCT01611597 Completed - Clinical trials for Neuromuscular Disease

Continuous Measurement of the Activity for Clinical Evaluation at Home, for Non-ambulant Neuromuscular Patients

Pre-Acti
Start date: January 2012
Phase: N/A
Study type: Interventional

Validation of a measure specifically suitable to evaluate the residual function of upper limbs of non-ambulant neuromuscular patients, especially with Duchenne muscular dystrophy and spinal muscular atrophy. This approach is of fundamental importance for clinical monitoring and preparing the future therapeutic trials.

NCT ID: NCT01569217 Enrolling by invitation - Respiratory Failure Clinical Trials

Regional Distribution of Ventilation to Assess Respiratory Muscle Dysfunction

DREM
Start date: June 2011
Phase: N/A
Study type: Observational

The aim of this study is to better discriminate respiratory muscle dysfunction by comparing the measurements of thoracoabdominal motion obtained by an optoelectronic recording and the conventional tests of respiratory muscle strength. The final objective is to better select in the future the patients who need more specific assessment of diaphragmatic function like "maximal transdiaphragmatic pressure" measurement and "phrenic nerve stimulation".

NCT ID: NCT01563705 Recruiting - Clinical trials for Neuromuscular Disorders

Prospective Follow-up of Patients With Glycogen Storage Disease Type III

PRO GSDIII
Start date: February 2011
Phase: N/A
Study type: Interventional

The aim of this study is to improve knowledge of natural history and methods of monitoring the evolution of Glycogen storage disease type III regarding the muscle and to study the prospective approach of large series of patients, and using the same protocol for the follow up of the children and adults.

NCT ID: NCT01560741 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Telemedicine and Ventilator Titration in Chronic Respiratory Patients Initiating Non-invasive Ventilation

TeleMotiNIV
Start date: July 2012
Phase: Phase 1
Study type: Interventional

The critical nature of respiratory diseases, the continuously increasing prevalence of these conditions, and the subjective perception of patients vis-à-vis their pulmonary function and health status underscore the importance of home telemonitoring. These conditions are critical and necessitate close and regular monitoring that may be achieved at distance using telemonitoring. This study will assess a number of measures both at baseline and post-intervention from a number of domains, including Arterial Blood Gases (ABG), BiPAP-related data, chronic respiratory failure symptoms, health-related quality of life, patients satisfaction and utilization of healthcare resources.

NCT ID: NCT01555905 Terminated - Clinical trials for Neuromuscular Disease

Respiratory Muscle Strength in Patients With NMD

RMST
Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if inspiratory muscle strength training (IMST) will impact maximal inspiratory pressure and pulmonary function in patients with neuromuscular disease.

NCT ID: NCT01519388 Completed - Respiratory Failure Clinical Trials

Evaluation of the Impact on Swallowing of Non Invasive Ventilation

OPTIDEG
Start date: February 2012
Phase: N/A
Study type: Interventional

Neuromuscular disorders can be associated with swallowing dysfunction secondary to a dysfunction of the airway muscles involved in swallowing. The investigators have shown that respiratory failure may contribute to swallowing dysfunction in patients with neuromuscular respiratory failure. Furthermore, although tracheostomy has been reported as impairing swallowing, the investigators have shown that when a tracheostomy is performed in neuromuscular patients, swallowing improves because it allows the patient to feed while ventilated. The investigators now want to evaluate whether non invasive ventilation may have a beneficial impact on swallowing by making some adjustments to ensure a good synchronisation between ventilation and swallowing. This could allow avoiding the necessity of a tracheostomy or a gastrostomy due to swallowing dysfunction and/or malnutrition in neuromuscular patients. Swallowing improvement under mechanical ventilation depends on improving the synchronisation between the patient and the ventilator during swallowing. For that purpose, the investigators developed a prototype ventilator able to temporarily suspend pressurisation under the patient's control so that when the patient needs to swallow under mechanical ventilation he may do so with an inadequate insufflation of the ventilator. Our objective is to to demonstrate that swallowing is more adapted and easier under nasal noninvasive ventilation than during spontaneous breathing in neuromuscular patients requiring prolonged noninvasive ventilation. In an open monocentric pilot study, the investigators will study 10 neuromuscular patients usually noninvasively ventilated. The patients will be their own control and their swallow will be studied during spontaneous breathing and under ventilation with the adapted ventilator while swallowing boluses of different volumes.

NCT ID: NCT01518439 Completed - Clinical trials for Chronic Respiratory Failure

Instrumental and Manual Increase of Couch in Neuromuscular Patients

OPTICOUGH
Start date: January 2012
Phase: N/A
Study type: Interventional

Inefficient cough is responsible of respiratory complications in neuromuscular patients which can lead to hospitalisation and can be life threatening. Techniques enhancing cough efficiency are successful in improving the clearance of bronchial secretions and help non invasive ventilation efficiency especially in case of acute respiratory failure. Combining mechanical exsufflation to the manual techniques of physiotherapy might enhance efficiency. Therefore the investigators want to compare cough efficiency under different techniques of instrumental and manual of cough assistance in order to determine the best combination to optimize cough flow.

NCT ID: NCT01495390 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

A Longitudinal Study of Amyotrophic Lateral Sclerosis (ALS) Biomarkers

Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of this study is to collect biofluid samples for the banking and usage in ALS research. Through comparison of these samples, the researchers hope to learn more about the underlying cause of ALS, as well as find unique biological markers, which could be used to develop new therapies.