Clinical Trials Logo

Multiple Sclerosis clinical trials

View clinical trials related to Multiple Sclerosis.

Filter by:

NCT ID: NCT02606630 Terminated - Multiple Sclerosis Clinical Trials

[11C]-PBR28 Positron Emission Tomography Study to Evaluate the Effect of ABT 555 in Subjects With Relapsing Forms of Multiple Sclerosis

Start date: October 2015
Phase: Phase 1
Study type: Interventional

This open-label positron emission tomography (PET) study is designed to determine the effect of ABT-555 on translocator protein expression level in participants with relapsing forms of multiple sclerosis.

NCT ID: NCT02580669 Terminated - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

Study by Magnetic Resonance Imaging in the Progressive Forms of Multiple Sclerosis

VASOSEP
Start date: June 16, 2014
Phase: N/A
Study type: Interventional

The goal of this study is to show pattern differences of vasoreactivity and connectivity between Progressive Multiple Sclerosis and Relapsing Remitting Multiple Sclerosis, by the use of methods of advanced brain MRIs and the Diffusion Tensor Imaging , and correlate these differences with Clinical disability and cognitive disorder results.

NCT ID: NCT02575365 Terminated - Cognition Clinical Trials

Effect of Fingolimod on Neurodegeneration

Start date: February 16, 2016
Phase: Phase 4
Study type: Interventional

This was a 24-month, open-label, multicenter study with a single treatment arm design. Primary objective of this study was: -To investigate the effects of Fingolimod on cognitive performance in highly active relapsing remitting multiple sclerosis patients Secondary objectives of this study were: - To investigate the correlation between the effect of fingolimod on cognitive performances and MRI data. - To evaluate the effect of fingolimod on biomarkers (24 hydroxy cholesterol, osteopontin and matrix metalloproteinases) related to neurodegeneration - To investigate the effect of fingolimod on brain gray matter atrophy and thalamic atrophy. Polulation The hope was to recruit a minimum of 80 relapsing remitting MS (RRMS) patients according to the McDonald criteria.

NCT ID: NCT02525367 Terminated - Multiple Sclerosis Clinical Trials

Online Cognitive Training in PD, MS and Depressed Patients Treated With Electroconvulsive Therapy

Start date: March 2016
Phase: N/A
Study type: Interventional

In Parkinson's disease, Multiple Sclerosis and depressed patients treated with electroconvulsive therapy, cognitive dysfunction is prevalent. However, treatment of these dysfunctions is in its infancy. The purpose of this study is 1) to assess the feasibility of a randomized controlled trial using an online computerized intervention for training cognitive abilities in the three patient groups and 2) to estimate the effect of the online training on objectively and subjectively measured cognitive functions. The investigators hypothesize that patients using online cognitive training will improve more on cognitive functions, as compared to patients using an active control condition.

NCT ID: NCT02466074 Terminated - Multiple Sclerosis Clinical Trials

Augmenting Cerebral Blood Flow to Treat Established Multiple Sclerosis

perfuseMS
Start date: August 17, 2016
Phase: Phase 2
Study type: Interventional

This study will evaluate how improved cerebral blood flow affects the way in which newly formed MS lesions evolve and whether tissue repair is improved. Patients with multiple sclerosis (MS) will be treated with acetazolamide in daily divided doses and obtain MRI to determine how much and in which regions of the brain cerebral perfusion improves as well as the extent to which tissue integrity is improved in these areas.

NCT ID: NCT02446886 Terminated - Multiple Sclerosis Clinical Trials

Adrenocorticotropic Hormone (ACTH) Effects on Myelination in Subjects With MS

Start date: June 2016
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine if monthly pulse doses of a three-day course ACTH (H.P. Acthar®) is more effective at recovering myelin at 12 months, as measured by myelin water fraction (MWF), in new multiple sclerosis lesions as compared to one course of treatment. The main secondary objective is to utilize every three month MWF measurements to determine the peak time of remyelination in new multiple sclerosis lesions when followed over the course of 12 months.

NCT ID: NCT02430532 Terminated - Clinical trials for Multiple Sclerosis, Secondary Progressive

BG00012 and Disability Progression in Secondary Progressive Multiple Sclerosis (SPMS)

INSPIRE
Start date: May 2015
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to investigate whether treatment with BG00012 (dimethyl fumarate) compared with placebo slows the accumulation of disability not related to relapses in participants with SPMS; The secondary objective of the study is to assess the effect of BG00012 compared with placebo on patient-reported outcomes, brain atrophy, and cognitive function.

NCT ID: NCT02428231 Terminated - Multiple Sclerosis Clinical Trials

Tecfidera Slow-titration Study

TITRATION
Start date: April 2015
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to assess whether a 6-week titration (compared with a 1-week titration) is effective in reducing the incidence of dimethyl fumarate (DMF)-related gastrointestinal (GI) Adverse Events (AEs) in subjects with Multiple Sclerosis (MS). The secondary objective of this study is to assess whether a 6-week titration (compared with a 1-week titration) is effective in reducing the average severity and duration of GI symptoms over 12 weeks of dimethyl fumarate treatment in this study population.

NCT ID: NCT02427776 Terminated - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

A Trial for Evaluating Both Safety and Preliminary Efficacy of a Single Infusion of Stimulated Autologous CD4+T Cells in Patients With Relapsing- Remitting Multiple Sclerosis

SCLEROLYM
Start date: January 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and the preliminary efficacy of a single infusion of stimulated autologous CD4+ T cells in patients with Relapsing-Remitting Multiple Sclerosis. The study duration for the patients (from start of baseline to end of follow-up) is 270 days.

NCT ID: NCT02423083 Terminated - Multiple Sclerosis Clinical Trials

Oral Guanabenz for Multiple Sclerosis

Start date: April 21, 2015
Phase: Phase 1
Study type: Interventional

Background: - People with multiple sclerosis (MS) get lesions in their brain and spinal cord. These cause neurological symptoms and sometimes disability. Researchers want to see if a blood pressure drug called guanabenz can repair lesions and help people with MS. Objective: - To see if guanabenz is safe and well tolerated in people with MS. Eligibility: - People 18 55 years old with MS who have taken glatiramer acetate for the past year. Design: - Participants will be screened in a separate protocol. For 2 months, they will be examined and have magnetic resonance imaging (MRI) scans. This will decide if they are in the Stable or Active MS study group. - The study will last 5 months. There will be up to 11 visits, 5 overnight. - Visit 1: overnight stay at the clinic: - Medical history and physical exam. - Health questionnaire - Bladder ultrasound scan - Brain MRI - Electrocardiogram (EKG) to measure heart electrical activity - Blood will be drawn through an intravenous (IV) line. - Participants may have tests of strength, muscle tone, and movement. - They will get their first dose of the study drug, a tablet taken once a day. - Participants will take the study drug at home and keep a medicine diary. - The dose will slowly increase. Each time, participants will stay overnight at the clinic. They will have a physical exam, EKG, MRI, and IV blood draw. - Visit 6: Participants will have a physical exam, MRI, and blood drawn. They will get a schedule to slowly lower their drug dose and stop taking guanabenz. - Participants will have 2 final visits. They will have a physical exam, EKG, MRI, and IV blood draw.