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ALS clinical trials

View clinical trials related to ALS.

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NCT ID: NCT01124292 Completed - Spinal Cord Injury Clinical Trials

Evaluation of a Tongue Operated Assistive Technology for Individuals With Severe Paralysis

TDS-1
Start date: May 2010
Phase: Phase 1
Study type: Interventional

This study was intended to evaluate a new assistive neuro-technology, known as the Tongue Drive System (TDS), by its potential end-users, i.e. individuals with severe disabilities, who are the best experts for indicating the benefits and possible shortcomings of any new ANT. Our goal is to assess the acceptability and usability of the TDS for various tasks that are important in daily lives of these individuals, such as computer access, wheeled mobility, and environmental control.

NCT ID: NCT01035476 Completed - ALS Clinical Trials

Optimizing NIPPV Use for Patients With ALS

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

This research will examine the utility of the data card recording capacity of nasal ventilation devices (NIPPV) in people with ALS to optimize use.

NCT ID: NCT00809224 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Cortex Changes in Real/Imagined Movements in Amyotrophic Lateral Sclerosis (ALS)

Start date: May 2008
Phase: N/A
Study type: Observational

The purpose of this study is to track areas of the brain, via functional magnetic resonance imaging (fMRI), that retain structural and functional integrity throughout the lifespan of people with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease.

NCT ID: NCT00696332 Completed - ALS Clinical Trials

Talampanel for Amyotrophic Lateral Sclerosis (ALS)

ALS
Start date: September 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, tolerability and safety of oral administration of talampanel compared to a placebo in subjects with ALS.

NCT ID: NCT00349622 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Clinical Trial Ceftriaxone in Subjects With ALS

Start date: July 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the safety and efficacy of ceftriaxone treatment in amyotrophic lateral sclerosis (ALS).

NCT ID: NCT00340301 Completed - ALS Clinical Trials

Exposure to Neurotoxins as Risk Factors for ALS

Start date: June 3, 2003
Phase:
Study type: Observational

Chemicals called neurotoxins can harm the nervous system. Amyotrophic lateral sclerosis (ALS) is a progressive disease affecting movement. Researchers have studied many possible causes of ALS, including injury, diet, and exposure to chemicals, but these studies were inconclusive. The purpose of this study was to determine whether exposure to lead or other neurotoxins can contribute to ALS. The study also evaluated lifestyle and dietary patterns. The study was completed in 1994-1996. One hundred eighty-two participants took part in this study 110 patients with ALS and 72 who did not have ALS. Each completed a questionnaire concerning lifestyle, diet, and residential, job, and medical history. Participants contributed 50 cc of blood, used to measure lead, as well as clippings of their toenails, used to measure mercury and other metals. They then underwent an XRF test (an X-ray procedure) to measure the level of lead in their shinbones and knees. Genes related to ALS or susceptibility to lead exposure were also evaluated.

NCT ID: NCT00339976 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Exposure to Neurotoxins as Risk Factors for Amyotrophic Lateral Sclerosis

Start date: August 6, 2002
Phase: N/A
Study type: Observational

This study is a follow-up to an earlier study that examined the relationship of This study will examine whether exposure to neurotoxins, such as lead, mercury, solvents, and pesticides, can contribute to amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. The cause of this degenerative disease of the brain and spinal cord is not well understood. Some studies suggest that exposure to environmental neurotoxins may increase its risk. This follow-up study will examine the relationship of neurotoxin exposure to the interval between the diagnosis of ALS and death. It will also examine the possible roles of genetics, lifestyle and dietary factors in the disease. Information on ALS patients previously enrolled in the study will be used to examine this relationship. No new individuals will be enrolled in the study.

NCT ID: NCT00140452 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Phase II Study Using Thalidomide for the Treatment of ALS

Start date: February 2005
Phase: Phase 2
Study type: Interventional

The use of Thalidomide in patients with ALS who have disease progression.

NCT ID: NCT00076154 Completed - ALS Clinical Trials

National Registry of Veterans With Amyotrophic Lateral Sclerosis and DNA Bank

ALS Registry
Start date: January 2003
Phase: N/A
Study type: Observational

This study will identify living veterans with amyotrophic lateral sclerosis (ALS) through a national registry that is being developed. Diagnosis of ALS will be verified by study neurologists via medical record review. Registry participation includes a bi-annual telephone interview to collect functional status data.