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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT02962050 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Delineating Swallowing Impairment and Decline in ALS

Start date: May 31, 2017
Phase:
Study type: Observational

The purpose of this study is to 1) evaluate the discriminant ability of simple clinical markers to detect swallowing impairment in individuals with ALS, 2) develop and validate a minimally invasive clinical screening tool for use at multidisciplinary ALS clinics, and 3) determine the natural history of swallowing impairment and decline in ALS.

NCT ID: NCT02943850 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

CNS10-NPC-GDNF for the Treatment of ALS

Start date: April 1, 2017
Phase: Phase 1
Study type: Interventional

The investigator is examining the safety of transplanting cells that have been engineered to produce a growth factor into the spinal cord of patients with Amyotrophic Lateral Sclerosis (ALS). The cells are called neural progenitor cells, which are a type of stem cell that can become several different types of cells in the nervous system. These cells have been derived to specifically become astrocytes, which is a type of neuronal cell. The growth factor is called glial cell line-derived neurotrophic factor, or GDNF. GDNF is a protein that promotes the survival of many types of neuronal cells. Therefore, the cells are called "CNS10-NPC-GDNF." The investigational treatment has been tested in animals, but it has not yet been tested in people. In this study, we want to learn if CNS10-NPC-GDNF cells are safe to transplant into the spinal cords of people.

NCT ID: NCT02942953 Completed - Clinical trials for Spinal Cord Injuries

Diaphragmatic Pacer Placement: Anesthetic Management (DP)

DP
Start date: June 2015
Phase: N/A
Study type: Observational [Patient Registry]

The diaphragmatic pacemaker (DP) has proven its utility in replacing mechanical ventilation (MV) in patients with chronic spinal cord injury (SCI) and Amyotrophic Lateral Sclerosis (ALS), by improving the patients quality of life and reducing morbi-mortality and the associated health care costs. The anesthetic management of these patients and the particularities of the surgical procedure represent an anesthetic challenge. The objective of our study is to analyze the management and the intraoperative complications in the patients with DP in our institution.

NCT ID: NCT02936635 Completed - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

A Study for Patients Who Completed VITALITY-ALS (CY 4031)

VIGOR-ALS
Start date: October 17, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the long-term safety and tolerability of tirasemtiv in patients with ALS who had completed the double-blind placebo-controlled study of tirasemtiv in ALS (CY 4031).

NCT ID: NCT02916966 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Environmental Exposure and Neurological Diseases Questionnaire

Cleveland Ohio
Start date: October 2016
Phase:
Study type: Observational

The proposed research is particularly relevant to the National ALS Registry and public environmental health issues because it addresses the potential environmental causes of sporadic ALS. The research will develop an ALS surveillance program in Ohio that can be compared with the national and State-Metro Surveillance Programs of the National ALS Registry, and novel methodologies to determine the role of the cyanobacterial toxin, BMAA (beta-methylamino-L-alanine), and other environmental toxins/toxicants as risk factors for ALS. This work will advance the mission of the Centers for Disease Control Agency for Toxic Substances and Disease Registry (CDC ATSDR) National ALS Registry by offering data on ALS cases in Ohio that address public health concerns over the effects of chronic exposure to cyanobacterial blooms in Lake Erie.

NCT ID: NCT02893605 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Study of Gene Polymorphisms Involved in the Metabolism and Action of Vitamin D in Amyotrophic Lateral Sclerosis

SLA_Vit_D
Start date: March 2014
Phase: N/A
Study type: Observational

This is a case-control study performed on a biological collection. The polymorphisms present on a pre-defined list of genes will be studied for 400 Amyotrophic Lateral Sclerosis (sporadic type) DNA samples and 400 control DNA samples.

NCT ID: NCT02891629 Completed - Clinical trials for ALS (Amyotrophic Lateral Sclerosis)

Safety and Feasibility of the EyeControl Device

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

The EyeControl device is an eye movement-based communication device in the form of wearable glasses with connected infrared cam-era that tracks the pupil and translates blinks and movements into commands.This study is aimed to demonstrate the safety and feasibility of the EyeControl device in healthy volunteers, and ALS patients in early stages.

NCT ID: NCT02880033 Completed - Parkinson's Disease Clinical Trials

Oxidative Stress and Apoptosis of Energy Metabolism by Deferiprone From the Circulating Lymphocytes

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

Peripheral blood mononuclear cells (PBMC) and platelets could be interesting ex vivo models to study brain diseases. Indeed, there is no access to neurons from patients. However, PBMC can exhibit different physiopathological mechanisms that are ubiquitous (i.e. oxidative stress, mitochondriopathy with energy metabolism, inflammation, protein folding, iron metabolism and programmed cell death ...). The platelets are pivotal in the healing system with large range of growth factors. A new therapeutic concept of conservative iron chelation with deferiprone for neuroprotection is under development. The action of deferiprone on the different mechanisms and notably the oxidative stress are to obtain from a collection of PBMC and platelets from patient having Parkinson's disease and Amyotrophic lateral sclerosis and healthy controls to study ex vivo. PBMC and platelets will be stored for future analyses.

NCT ID: NCT02872142 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Efficacy and Safety of Plasma Exchange With Albutein® 5% in Participants With Amyotrophic Lateral Sclerosis

Start date: August 29, 2016
Phase: Phase 2
Study type: Interventional

This is a pilot, phase 2, prospective, open-label, single-arm study to evaluate disease progression, forced vital capacity, and the safety and tolerability of plasma exchange (PE) using Albutein® 5% in participants with amyotrophic lateral sclerosis (ALS).

NCT ID: NCT02870634 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Phase 1 Dose Escalation and PK Study of Cu(II)ATSM in ALS/MND

Start date: November 16, 2016
Phase: Phase 1
Study type: Interventional

Multicenter, open-label , single and multiple dose-escalation and pharmacokinetic study