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Neuromuscular Diseases clinical trials

View clinical trials related to Neuromuscular Diseases.

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NCT ID: NCT03218215 Completed - Clinical trials for Neuromuscular Diseases

Monitoring Mechanical Assisted Cough

MONICA
Start date: May 1, 2015
Phase: N/A
Study type: Observational

Background Mechanical assistance cough for patients with neuromuscular disorders (NMD) are known, but there is no adaptation model established. Currently is performed subjectively by the physiotherapist following the pressures recommended in the current literature as optimal (±40CmH2O). To check is these pressures are the most optimal pressures to achieve the better peak cough flow (PCF) monitoring cough assist (Mechanical insuffllation-exsuflattion MI-E) maneuvers and analyzing pressure- flow / time curves Adults with MI-E criteria (PCFbaseline <160 l /min). A pneumotachograph, PeakAnalysis software and nasobucal mask were used to monitor and analyze flow/time curves. Protocol included 9 PCF values in each patient: 1 baseline, 4 related with inspiratory pressure in sequential increase of 10 cmH2O (10 to 40 cmH2O) and 4 adding expiratory pressures (±10 to ±40cmH2O)

NCT ID: NCT03212846 Completed - Spasticity, Muscle Clinical Trials

Muscle Spasticity Reduction in Children With Cerebral Palsy by Means of Hippotherapy

Start date: June 2016
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate if a intervention with hippotherapy will improve spasticity for children ages 3-14 who have cerebral palsy. The hip aductors spasticity will be measured using the Modified Ashworth Scale (MAS). The intervention will be performed in addition to traditional treatment.

NCT ID: NCT03203577 Completed - Clinical trials for Neuromuscular Diseases

Initiation of Home Mechanical Ventilation at Home in Patients With Chronic Hypercapnic Respiratory Failure

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

Objective: To prove that initiation of chronic ventilatory support at home, in patients with chronic hypercapnic respiratory failure due to neuromuscular disease (NMD) or thoracic cage problem is not inferior compared to initiation in a hospital based setting. In addition we believe that the start at home is cheaper compared to an in-hospital start. Hypothesis: Initiation of chronic ventilatory support at home is effective, safe and cost effective compared to a hospital-based initiation. Study design: A nationwide non-inferiority multi-center randomized parallel active control study. Study population: Patients with chronic respiratory insufficiency due to a neuromuscular disease (NMD) or thoracic cage problem who are referred for chronic ventilator support. Intervention: The start of HMV at home Standard intervention to be compared to: The start of HMV is normally in a clinical setting as recommended in the national guideline. Outcome measures: Primary: PaCO2. Secondary: Health related quality of life; lung function; nocturnal transcutaneous carbon dioxide assessment and saturation, and costs Sample size calculation/data analysis: This is a non-inferiority trial based on PaCO2 as primary outcome. A difference in favor of the hospital care group of smaller than 0.5 kPa will be labeled as non-inferior. To retain 72 evaluable patients, and allow for drop-outs, we will include 96 patients in total. Cost-effectiveness analysis: A cost analysis will be conducted alongside the clinical trial. Costs of the initiation of HMV at home and in the hospital will be estimated form a societal perspective over a time horizon of 6 months. Time schedule: After an initial phase of 6 months recruitment will start and will take 24 months. Thirty-six months after the start of the study the last assessments will be done and analysis and writing of the papers will start. After 42 months the study will end.

NCT ID: NCT03179631 Completed - Clinical trials for Nervous System Diseases

Long-Term Outcomes of Ataluren in Duchenne Muscular Dystrophy

Start date: July 6, 2017
Phase: Phase 3
Study type: Interventional

This study is a long-term study of ataluren in participants with nonsense mutation Duchenne muscular dystrophy.

NCT ID: NCT03127514 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

AMX0035 in Patients With Amyotrophic Lateral Sclerosis (ALS)

CENTAUR
Start date: June 22, 2017
Phase: Phase 2
Study type: Interventional

The CENTAUR trial was a 2:1 (active:placebo) randomized, double-blind, placebo-controlled Phase II trial to evaluate the safety and efficacy of AMX0035 for the treatment of ALS.

NCT ID: NCT03116620 Completed - Clinical trials for Mastication Disorder

Chewing Function in Pediatric Neuromuscular Disorders

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

We aimed to evaluate chewing function (CF) in children with neuromuscular disorders, and investigate reliability of the Karaduman Chewing Performance Scale (KCPS).

NCT ID: NCT03085537 Completed - Clinical trials for Neuromuscular Diseases

Effectiveness Monitoring of Home Non-invasive Mechanical Ventilation by Digital Diagnosis Platform

PRE-HVNI
Start date: October 1, 2016
Phase:
Study type: Observational [Patient Registry]

The main objective will be to determine the effectiveness of home non-invasive ventilation by flow-time and time-pressure curves analysis in a cohort of patients with this treatment by digital diagnosis platform.

NCT ID: NCT03038906 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Effect of Randomization to Neuromuscular Blockade on Physical Functional Impairment and Recovery in ARDS

PRIMROSE
Start date: January 2017
Phase: N/A
Study type: Observational

The proposed work will determine the effect of neuromuscular blockade on physical function and recovery in patients with ARDS. The investigators will conduct a prospective ancillary study at five PETAL clinical centers that will evaluate the neuromuscular structure and function of ROSE (Reevaluation of Systemic Early Neuromuscular Blockade) patients during and after critical illness, including in-person assessments at 6 months after hospital discharge. The investigators hypothesize that patients randomized to NMB will have an increase in ICU-acquired neuromuscular dysfunction during and after critical illness.

NCT ID: NCT03032562 Recruiting - Clinical trials for Respiratory Muscle Paralysis

Respiratory Muscle Strength and Function in Neuromuscular Disorders and Chronic Obstructive Pulmonary Disease

Start date: December 1, 2016
Phase: N/A
Study type: Observational

Using an extensive set of both volitional and non-volitional tests of respiratory muscle function and strength it is the aim of this study to - identify disease-specific patterns of respiratory muscle impairment in different NMD and COPD - establish which set of tests is predictive of sleep-disordered breathing or daytime hypercapnia in patients with NMD or COPD, respectively. - to investigate the decline of respiratory muscle function in patients with progressive NMD and COPD along with sleep studies and capnography

NCT ID: NCT02997514 Active, not recruiting - Clinical trials for Neuromuscular Diseases

Solution Focused Coaching Strategy Within a Paediatric Multidisciplinary Neuromuscular Clinic

Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to implement Solution Focused Coaching in pediatric rehabilitation (SFC-peds) within the multidisciplinary neuromuscular clinic at Holland Bloorview Kids Rehabilitation Hospital and evaluate its effect on children's ability to set and attain personally meaningful goals. A secondary goal is to determine the impact of SFC-peds on self-determination in children with neuromuscular conditions. This study aims to compare two methods of SCF-peds delivery, a single coaching session vs. intensive coaching (5 sessions) on goal attainment. This study will also help researchers and clinicians understand the types of goals that are set by children with neuromuscular conditions. Lastly, this study is going to explore with the participants their perception of the feasibility of using this methodology within a clinical context.