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Sclerosis clinical trials

View clinical trials related to Sclerosis.

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NCT ID: NCT00289159 Active, not recruiting - Multiple Sclerosis Clinical Trials

Multimodal MRI in Multiple Sclerosis (MS): Reliability and Follow Up

Start date: n/a
Phase: Phase 4
Study type: Observational

To determine wether multimodal MRI (conventinal T1 and T2 sequences, diffusion, magnetization transfer, spectroscopy) is reproducible; to follow up a cohort of patients with early remmittent MS after treatment with interferon.

NCT ID: NCT00127075 Active, not recruiting - Multiple Sclerosis Clinical Trials

POPART'MUS: Prevention of Post Partum Relapses With Progestin and Estradiol in Multiple Sclerosis

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

Multiple sclerosis (MS) affects 1 in 1000 people in western countries, mainly women in their childbearing years. It is an autoimmune disease of the central nervous system (CNS), which results in a chronic focal inflammatory response with subsequent demyelination and axonal loss. Recent prospective studies reported a significant decline by two-thirds in the rate of relapses during the third trimester of pregnancy and a significant increase by two-thirds during the first three months post-partum by comparison to the relapse rate observed during the year prior to the pregnancy (Confavreux et al., 1998). These dramatic changes in the relapse rate occur at a time when the impregnation of many substances (among which, sexual steroids) is at its highest, before a dramatic decline to the pre-pregnancy levels, immediately following delivery. It may be hypothesized that sexual steroids could exert beneficial effects through a modulation of the immune state with a lowering of the pro-inflammatory lymphocyte responses of the Th1 type and an enhancement of the anti-inflammatory responses of the Th2 type. They may also play a direct role in the remyelination of central nervous system lesions, as they do in the peripheral nervous system. The POPART'MUS study is a European, multicentre, randomized, placebo-controlled and double-blind clinical trial, which aims to prevent MS relapses related to the post-partum condition, by administering high doses of progestin (nomegestrol acetate), in combination with endometrial protective doses of estradiol. Treatment will be given immediately after delivery and continuously during the first three months post-partum. Assuming the results of the trial to be positive, this new treatment could be considered in the relapsing-remitting phase of the disease in women afar from pregnancy and post-partum.

NCT ID: NCT00069186 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Study of Creatine Monohydrate in Patients With Amyotrophic Lateral Sclerosis

Start date: June 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether nine months of administration of creatine monohydrate results in an increase in muscle strength in patients with amyotrophic lateral sclerosis (ALS).

NCT ID: NCT00004645 Active, not recruiting - Clinical trials for Acute Disseminated Encephalomyelitis

Phase III Randomized, Double-Blind, Sham-Controlled Study of Plasma Exchange for Acute Severe Attacks of Inflammatory Demyelinating Disease Refractory to Intravenous Methylprednisolone

Start date: January 1995
Phase: Phase 3
Study type: Interventional

OBJECTIVES: I. Evaluate the effectiveness of plasma exchange in the treatment of acute severe attacks of inflammatory demyelinating disease in patients who have failed intravenous steroid therapy.

NCT ID: NCT00004457 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Determinants of Disease Severity in Amyotrophic Lateral Sclerosis

Start date: March 1998
Phase: N/A
Study type: Observational

OBJECTIVES: I. Determine specific clinical features, molecular abnormalities, and laboratory-based biological markers of free radical stress that are associated with amyotrophic lateral sclerosis and influence disease severity.