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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT01041222 Completed - Clinical trials for Familial Amyotrophic Lateral Sclerosis

Safety, Tolerability, and Activity Study of ISIS SOD1Rx to Treat Familial Amyotrophic Lateral Sclerosis (ALS) Caused by SOD1 Gene Mutations

SOD-1
Start date: January 2010
Phase: Phase 1
Study type: Interventional

This study will test the safety, tolerability and pharmacokinetics of single doses of ISIS 333611 administered into the spinal canal as 12 hour infusions.

NCT ID: NCT01020331 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Memantine Therapy in Amyotrophic Lateral Sclerosis

TAME
Start date: June 2005
Phase: Phase 2
Study type: Interventional

Tau, a protein in the cerebrospinal fluid CSF is believed to be elevated in amyotrophic lateral sclerosis (ALS) patients. The investigators believe that Tau is truly a marker of increased neuronal death from any disease process. It is been shown that Memantine can inhibit and reverse the abnormal hyperphosphorylation of Tau and therefore the investigators are looking at the efficacy of Memantine at 10 mg twice a day (BID) to see if disease progression correlates with possible changes in Tau in ALS patients based on ALS Functional Rating Scale (ALSFRS) scores.

NCT ID: NCT00983983 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

High Fat/High Calorie Trial in Amyotrophic Lateral Sclerosis

Start date: October 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, and preliminary efficacy of long-term use of high fat/high calorie and high calorie diets in people with amyotrophic lateral sclerosis (ALS) (Lou Gehrig's disease).

NCT ID: NCT00965497 Completed - Multiple Sclerosis Clinical Trials

Escitalopram (Lexapro) for Depression MS or ALS

Start date: July 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if escitalopram (Lexapro) improves symptoms of major depressive disorder in patients who have ALS or MS.

NCT ID: NCT00958048 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Effects of Nocturnal Non-invasive Ventilation in Patients With Amyotrophic Lateral Sclerosis

Start date: January 2009
Phase: N/A
Study type: Interventional

Specific aims: Aim 1. To determine the incidence of hypoventilation in Amyotrophic Lateral Sclerosis (ALS) patients. Aim 2. To identify the clinical characteristics and risk factors associated . Aim 3. To determine the effect of early intervention with nocturnal NIV on the prognosis of ALS patients.

NCT ID: NCT00956501 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Assessment of Postural Orientation and Equilibrium In Early Amyotrophic Lateral Sclerosis (ALS)

Start date: February 2009
Phase:
Study type: Observational

The purpose of this pilot study is to characterize changes in postural orientation and equilibrium in early diagnosed ALS patient. The investigators plan to cross validate the use of a standardized test of equilibrium (EquiTest, Computerized Dynamic Posturography - CDP) in early diagnosed ALS patients.

NCT ID: NCT00956488 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Supported Treadmill Ambulation Training (STAT) for Patients Diagnosed With Amyotrophic Lateral Aclerosis

Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find out if supervised exercise training using a treadmill with partial weight support is safe and has an impact on gait and function of persons with Amyotrophic lateral sclerosis.

NCT ID: NCT00931944 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Open-Label, Safety and Tolerability Extension Study of KNS-760704 in Amyotrophic Lateral Sclerosis (ALS) (CL211)

CL211
Start date: July 2009
Phase: Phase 2
Study type: Interventional

This is an open-label, multi-center study designed to extend the evaluation of the safety, tolerability, and clinical effects of oral administration of KNS-760704 in patients with ALS.

NCT ID: NCT00925847 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Effect of Lithium Carbonate in Patients With Amyotrophic Lateral Sclerosis

LISLA
Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether lithium is safe and effective in the treatment of ALS

NCT ID: NCT00919555 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Combination Therapy in Amyotrophic Lateral Sclerosis (ALS)

PNA
Start date: June 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to determine the safety and the efficacy of Tretinoin and Pioglitazone HCL in patients with ALS who are currently on Riluzole.