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Sclerosis clinical trials

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NCT ID: NCT00331747 Recruiting - Multiple Sclerosis Clinical Trials

Gait Evaluation in Multiple Sclerosis Patients Treated With Glatiramer Acetate

Start date: May 2006
Phase: N/A
Study type: Interventional

Hypothesis: Treatment with Glatiramer acetate prevents deterioration of gait in multiple sclerosis (MS) patients. During the study patients will undergo a 3 dimensional gait analysis before starting treatment with glatiramer acetate and after 1 year of treatment.

NCT ID: NCT00317616 Recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

The Pre-symptomatic Familial Amyotrophic Lateral Sclerosis (Pre-fALS) Study

Pre-fALS
Start date: April 2006
Phase:
Study type: Observational

Pre-fALS is a prospective natural history and biomarker study of people not yet affected with ALS, but who are at genetic risk for developing ALS. The investigators aim to recruit unaffected (healthy) people from familial ALS (fALS) pedigrees in which a known genetic mutation associated with ALS has been identified; for this study, a fALS pedigree is one with two biologically related individuals who have or have had ALS and/or FTD. Individuals who may be at genetic risk for ALS and who belong to families with at least one affected family member who has tested positive for a known ALS genetic mutation may also be eligible to participate. Our goal is to study the pre-symptomatic phase, onset and progression of ALS and to learn more about genetic and environmental factors that put people at risk for developing ALS.

NCT ID: NCT00242268 Recruiting - Clinical trials for Relapsing Remitting Multiple Sclerosis

A Safety Study of Combination Treatment With Avonex and Zocor in Relapsing Remitting Multiple Sclerosis

Start date: October 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if using Avonex in combination with Zocor is a safe and effective therapy for subjects with relapsing remitting multiple sclerosis.

NCT ID: NCT00230204 Recruiting - Multiple Sclerosis Clinical Trials

Infections and Autoimmunity: Autobodies Screening in Multiple Sclerosis

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The purpose of this investigation is to assess the prevalence of infectious disease seropositivity (toxoplasmosis, rubella, cytomegalovirus [CMV]), herpes simplex virus type 1 (HSV-1) and herpes simplex virus type 2 (HSV-2), syphilis, Epstein-Barr virus and H. pylori in a group of patients presenting with specific autoimmune diseases (rheumatoid arthritis [RA], undifferentiated connective tissue disorder [UCTD], Sjogren, antiphospholipid syndrome - APS, vasculitides, systemic lupus erythematosus [SLE], polymyositis, Hashimoto, multiple sclerosis, primary biliary cirrhosis [PBC], etc.), using the BioPlex 2200 and complementary EIA kits as compared to matched controls (by age, sex and ethnicity).

NCT ID: NCT00228228 Recruiting - Multiple Sclerosis Clinical Trials

TCV -01-002: T-Cell Vaccination in the Treatment of Probable Multiple Sclerosis

Start date: May 2002
Phase: Phase 3
Study type: Interventional

In the present study, we, the investigators at Sheba Medical Center, intend to evaluate T cell vaccination (TCV) in patients with probable multiple sclerosis (MS) within up to 3 months after the first clinical attack. It is of the utmost importance to evaluate the treatment effects at the onset of disease, i.e. in patients with probable MS, in order to evaluate whether early treatment can prevent the second attack (conversion to definite MS). Moreover, at disease onset, the immunological process of epitope spreading associated with the exposure of the immune system to myelin antigens is still limited. With additional attacks, increased recognition of new self-determinants of encephalitogenic peptides presented to the immune system during the inflammatory process occurs, and enhances further disease activity. The aim of the early TCV treatment approach is to stop this process as early as possible, during the onset of the disease, thus preventing additional attacks and disease progression. We will evaluate the effect of TCV on clinical, immunological and magnetic resonance imaging (MRI) parameters in patients with probable MS.

NCT ID: NCT00220506 Recruiting - Clinical trials for All Multiple Sclerosis Patients

Fatigue Treatment Using Provigil

Start date: September 2005
Phase: N/A
Study type: Interventional

To determine whether therapy with Modafinal(Provigil) is safe and effective in fatigue in MS Patients

NCT ID: NCT00220493 Recruiting - Clinical trials for Relapsing Remitting Multiple Sclerosis

Evaluation of Efficiency of Ritalin in Multiple Sclerosis (MS) Patients

Start date: June 2003
Phase: Phase 1
Study type: Interventional

Scientific background: Growing awareness and accumulating data regarding the cognitive impairment and its progression in multiple sclerosis (MS) patients has received an important place in neurological research in the last decade.

NCT ID: NCT00220428 Recruiting - Multiple Sclerosis Clinical Trials

T-Cell Vaccination in Multiple Sclerosis (MS)

Start date: July 1998
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of T-cell vaccination in MS patients.

NCT ID: NCT00217295 Recruiting - Multiple Sclerosis Clinical Trials

A Safety Study of Combination Treatment With Avonex and Placebo-Controlled Dosing of Topamax in Relapsing-Remitting Multiple Sclerosis

Start date: April 2004
Phase: Phase 2
Study type: Interventional

This is a clinical trial in relapsing-remitting Multiple Sclerosis to determine if Topamax added to Avonex has a neuroprotective effect as measured by the brain parenchymal fraction ( a measure of brain shrinkage) and by clinical assessment scores to evaluate disease progression.

NCT ID: NCT00202423 Recruiting - Multiple Sclerosis Clinical Trials

Use of Cannabinoids in Patients With Multiple Sclerosis

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

This is a 10-week, randomised, double blind, placebo-controlled, crossover trial to investigate the effect of Cannabis Based Medicine Extract (Sativex) on patterns of brain activation associated with movement in 20 MS patients suffering from lower limb spasticity. Spasticity is a common symptom in Multiple Sclerosis (MS), occurring all over the course of the disease, particularly in the progressive phase.Physiologically, spasticity and hyperreflexia habitually seen in patients with pyramidal syndrome is due to lesions of other descending pathways, such as the cortico reticulospinal pathways, which participate in voluntary movements.It is now known that an endocannabinoid system acts in humans by at least two types of cannabinoids receptors, CB1 and CB2. There is evidence to support the view that the psychoactive ingredient in cannabis, delta 9-tetrahydrocannabinol (delta 9-THC), and cannabinoids in general, can reduce muscle spasticity in people with MS. Aim of the study will be to evaluate the effect of Sativex on: (i) patterns of brain activation associated with movement (fMRI) in MS patients suffering from spasticity; (ii) changes in level of spasticity (H-reflex); (iii) changes in intracortical excitability and on synaptic intracortical network of the motor areas (double shock TMS).