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Nervous System Diseases clinical trials

View clinical trials related to Nervous System Diseases.

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NCT ID: NCT00422955 Completed - Clinical trials for Neuropathy, Diabetic

Fluid Retention in Rosiglitazone Treated Subjects With Autonomic Neuropathy.

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

Fluid management study in patients with type 2 diabetes and autonomic neuropathy.

NCT ID: NCT00422474 Recruiting - Clinical trials for Cerebrovascular Accident

Prognostic Significance of the Baroreflex Sensitivity Changes After Acute Ischemic Stroke

Start date: January 2007
Phase: N/A
Study type: Observational

After acute stroke, baroreflex sensitivity (BRS) is impaired. This impaired acute stage BRS has been reported to be predictive of worsen outcome years after stroke in general. However, it is not very clear if the impaired acute stroke BRS would actually persist months after the acute stage. It is also not clear that such change, if any, would correlate with the functional outcome or prognosis after stroke. The trial is to investigate the longitudinal time course of BRS after ischemic stroke up to the 6th month post stroke and to see if there is any correlation of the changes in BRS with the functional outcome parameters using NIHSS and mRS scores throughout this period.

NCT ID: NCT00406029 Completed - Parkinson Disease Clinical Trials

Dyskinesia in Parkinson's Disease (Study P04501)

Start date: November 20, 2006
Phase: Phase 2
Study type: Interventional

The purpose of the study is to assess the efficacy and safety of a range of doses of SCH 420814 (preladenant) when used together with a stable dose of L-dopa/dopa decarboxylase inhibitor to treat Parkinson's disease. In this study, we will be comparing 3 doses (1 mg, 2 mg, and 5 mg taken twice a day) of preladenant with placebo (sugar pill). Following an Interim Analysis (temporary hold for new enrollment-ongoing subjects will continue on treatment) to review drug safety, a new dose group of 10 mg (taken twice a day) may be added. Approximately 160 participants will be randomized in this study in approximately 22 study centers worldwide for the first part of this study. Following the Interim Analysis, 40 new participants may be added, for a total of 200 participants. The study is double blind, which means neither you nor your study doctor will know whether you are receiving the study medication or placebo.

NCT ID: NCT00395460 Completed - Clinical trials for Central Nervous System Diseases

Efficacy and Safety Study to Evaluate Gadavist (Gadobutrol) as Contrast Agent in Magnetic Resonance Imaging (MRI) of Brain or Spine Diseases in Chinese Patients

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

The purpose of this study is to determine if the contrast agent is effective and safe in the Magnetic Resonance Imaging (MRI) of brain or spine diseases in patients of Chinese origin.

NCT ID: NCT00359632 Terminated - Clinical trials for Optic Nerve Diseases

Study to Evaluate Eye Function in Patients Taking Linezolid for Six Weeks or Greater

Start date: November 2008
Phase: Phase 3
Study type: Interventional

To understand and characterize the effects of linezolid on the optic nerve by observing and following patients who have been treated with linezolid for six weeks or longer for the development of signs or symptoms of visual disturbance or eye disorders.

NCT ID: NCT00348933 Completed - Clinical trials for Nervous System Diseases

Dietary Supplements for the Treatment of Angelman Syndrome

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

Angelman syndrome (AS) is a complex genetic disorder that affects the nervous system. The purpose of this study is to determine the effectiveness of certain dietary supplements in treating the symptoms of AS.

NCT ID: NCT00323310 Terminated - Clinical trials for Central Nervous System Diseases

Safety and Efficacy of MultiHance in Pediatric Patients

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

The purpose of this study was to assess the safety and enhancing properties of the magnetic resonance imaging (MRI) contrast agent MultiHance in children aged 2 to 17 years having central nervous system (CNS) disorders.

NCT ID: NCT00321672 Completed - Pain Clinical Trials

Study of NGX-4010 for the Treatment of Painful HIV-Associated Neuropathy

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

The purpose of the study was to assess the efficacy and safety of NGX-4010 applied for 30 or 60 minutes for the treatment of painful HIV-associated neuropathy.

NCT ID: NCT00304291 Completed - Clinical trials for Neuromyelitis Optica

A Pilot Study of Mitoxantrone for the Treatment of Recurrent Neuromyelitis Optica (Devic's Disease)

Start date: August 2001
Phase: Phase 4
Study type: Interventional

Neuromyelitis optica (NMO) is a severe demyelinating disease that selectively involves the optic nerves and the spinal cord but usually spares the brain. NMO is considered to have a B cell induced pathogenesis. Mitoxantrone (MITO, Novantrone®), a synthetic anthracenedione approved for worsening relapsing-remitting multiple sclerosis (MS) and secondary progressive MS, has been shown to primarily suppress the humoral response. We conducted a prospective 2-year study to evaluate the benefit of MITO in five relapsing NMO patients.

NCT ID: NCT00300222 Completed - Pain Clinical Trials

Study of NGX-4010 for the Treatment of Postherpetic Neuralgia

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

The purpose of the study is to assess the efficacy and safety of NGX-4010 applied for 60 minutes for the treatment of postherpetic neuralgia (PHN).