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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT01825551 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

The Effect of GCSF in the Treatment of ALS Patients

Start date: November 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the effect off Granulocyte Colony Stimulating Factor (GCSF) in the treatment of Amyotrophic Lateral Sclerosis (ALS) patients.

NCT ID: NCT01823380 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Influence of the Vitamin D Blood Levels on the Amyotrophic Lateral Sclerosis Phenotype

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

The main objective of this study is to investigate the correlation between the rate of motor decline and blood levels of Vitamin D total. Secondary objectives are to investigate the relationship between blood levels of vitamin D and total disease duration of ALS, forced vital capacity, weight loss, age of onset and the start site of ALS.

NCT ID: NCT01806857 Completed - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Clinical Trial Nuedexta in Subjects With ALS

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Nuedexta is effective in the treatment of symptoms (impaired speech, swallowing, and saliva control)associated with Amyotrophic Lateral Sclerosis (ALS).

NCT ID: NCT01786603 Completed - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Rasagiline in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Start date: November 21, 2013
Phase: Phase 2
Study type: Interventional

ALS is a disorder that weakens motor strength and lung function. Rapid loss of motor neurons in the brain and spinal cord of ALS patients causes the symptoms of increasing weakness and loss of muscle function. Motor neurons are responsible for sending signals to muscles in our bodies to trigger movement. While there are drugs to help relieve symptoms of ALS, there is no cure for ALS. Rasagiline is a drug with possible neuroprotective characteristics. Neuroprotective means that the nervous system may be protected against weakening. It is known that rasagiline has possible neuroprotective characteristics, but the effectiveness of rasagiline for patients with ALS has not been tested. Rasagiline is approved for the treatment of Parkinson's disease. Rasagiline for treatment of ALS is not approved by the U.S. Food and Drug Administration (FDA) and is investigational. Investigational drugs are studied to find out if they are safe and effective in the treatment of diseases or conditions. By doing this study, researchers hope to learn if rasagiline is safe and slows disease progression in patients with ALS. Funding Source - FDA OOPD (FDA Orphan Products Division).

NCT ID: NCT01786174 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Gilenya in Amyotrophic Lateral Sclerosis (ALS)

Start date: August 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Gilenya, also known as fingolimod, is safe and tolerable in patients with Amyotrophic Lateral Sclerosis (ALS).

NCT ID: NCT01777646 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Autologous Mesenchymal Bone Marrow Stromal Cells Secreting Neurotrophic Factors (MSC-NTF), in Patients With Amyotrophic Lateral Sclerosis (ALS)

Start date: December 2012
Phase: Phase 2
Study type: Interventional

The study will evaluate the safety, tolerability and therapeutic effects of transplantation of escalating doses of autologous cultured mesenchymal bone marrow stromal cells secreting neurotrophic factors (MSC-NTF), in patients with amyotrophic lateral sclerosis (ALS).

NCT ID: NCT01776970 Completed - Clinical trials for Motor Neuron Disease

Safety and Efficacy on Spasticity Symptoms of a Cannabis Sativa Extract in Motor Neuron Disease

CANALS
Start date: January 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The clinical primary hypothesis is that there will be a difference between a Cannabis Sativa extract and placebo in their effect on spasticity in Motor Neuron Disease (MND) patients with signs of involvement of the upper motor neuron (UMN) resulting in disabling spasticity. Secondary goals of the study are to evidence of improvement in other symptoms (in particular pain), and to show favourable trends on functionality measures. Finally, cannabis based drug safety and tolerability will be studied through vital parameters (including weight and pulmonary function) measurement, and analyzing ALS function rating scale progression slope hopefully, showing a slowing of the functional values decrease, owing to cannabis neuroprotective effects)

NCT ID: NCT01772888 Completed - Clinical trials for Amyotrophic Lateral Sclerosis 11

Chewing Efficiency Measured by a Two Colour Chewing Gum Test in Amyotrophic Lateral Sclerosis (ALS) Patients?

Start date: October 2012
Phase:
Study type: Observational

Study aims: The primary aim is to determine whether chewing efficiency, determined by a two-colour mixing ability test, and maximum bite and lip force decrease in ALS patients.

NCT ID: NCT01771640 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Intrathecal Transplantation of Mesenchymal Stem Cell in Patients With ALS

Start date: August 2013
Phase: Phase 1
Study type: Interventional

ALS is a debilitating disease with varied etiology characterized by rapidly progressive weakness, muscle atrophy and fasciculations, muscle spasticity, difficulty speaking (dysarthria), difficulty swallowing (dysphagia), and difficulty breathing (dyspnea). ALS is the most common of the five motor neuron diseases.Riluzole (Rilutek) is the only treatment that has been found to improve survival but only to a modest extent. It lengthens survival by several months, and may have a greater survival benefit for those with a bulbar onset. It also extends the time before a person needs ventilation support.Stem cell transplantation is a new hopeful way to improve the patients conditions and reduce the period of disabilities.

NCT ID: NCT01758510 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Safety Study of HLA-haplo Matched Allogenic Bone Marrow Derived Stem Cell Treatment in Amyotrophic Lateral Sclerosis

Start date: December 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety of HLA-haplo matched Allogenic Bone Marrow Derived stem cells("HYNR-CS-Allo inj"), through intrathecal delivery for the treatment in patients with amyotrophic lateral sclerosis(ALS). This study is an open label, dose up and down study using the 3+3 design to assess the safety of HLA-haplo matched Allogenic Bone Marrow Derived stem cells("HYNR-CS-Allo inj")