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Nervous System Diseases clinical trials

View clinical trials related to Nervous System Diseases.

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NCT ID: NCT02455284 Completed - Clinical trials for Neurological Diseases

In Vivo and ex Vivo Validation of MR Tractography of Brain White Matter Tracts - FIBRATLAS II-III

FIBRATLAS
Start date: October 2015
Phase: N/A
Study type: Interventional

White matter tracts connect cortical areas to other parts of the cortex, to basal ganglia and to the brain stem and spinal cord. These tracts form the internal part of the brain and transmit the nervous impulses. Changes in brain white matter may serve as biomarkers for numerous neurological diseases. Diffusion Weighted Imaging (DWI) is a non-invasive MRI (Magnetic Resonance Imaging) technique providing information on white matter tracts (tractography) by studying water diffusion. Since it is based on complex mathematical models that only indirectly evaluates the underlying anatomy, tractography need to be validated before being used for research and clinical purposes. Several validation techniques were previously proposed, none of them being fully convincing in human.

NCT ID: NCT02436096 Completed - Fibromyalgia Clinical Trials

A Study to Evaluate eFFIcacy and Safety of Sublingual TNX-102 SL Tablet Taken at Bedtime in Patients With fibRoMyalgia

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

The use of low-dose CBP dosed nightly at bedtime for FM was supported by the results of Tonix' TNX-CY-F202 Phase 2b study (also referred to as the BESTFIT Study). The TNX-CY-F202 study provided strong evidence that TNX-102 SL 2.8 mg dosed nightly results in beneficial effects upon pain, sleep and other FM symptomatology. The present trial is designed to assess the safety and efficacy of TNX-102 SL 2.8 mg tablets, taken daily at bedtime over 12 weeks to treat fibromyalgia.

NCT ID: NCT02435641 Completed - Clinical trials for Intensive Care Neurological Disorder

Patient and Caregiver Psychological Functioning Following Neuro-ICU Admission: A Prospective Investigation

Start date: March 2015
Phase:
Study type: Observational

The current study has the following objectives: 1. To determine predictors of time 2 and 3 (3 and 6 months post-ICU admission) depression, PTSD, satisfaction with life and quality of life in both patients and caregivers, after controlling for injury severity and impairment. 2. To determine factors associated with patient and caregiver satisfaction with medical care at time 2 and time 3. The investigators would thus be able to identify the best time point for intervention delivery, intervention targets, and risk factors for chronic psychological distress.

NCT ID: NCT02431780 Completed - Epilepsy Clinical Trials

A Multicentre Clinical Investigation of a Decision Support Algorithm for Neonatal Seizure Detection

ANSeR
Start date: February 12, 2015
Phase: N/A
Study type: Interventional

The ANSeR Clinical Investigation is a multi-centre, randomised, controlled, clinical investigation of a standalone decision support Algorithm for Neonatal Seizure Recognition, the ANSER Software system.

NCT ID: NCT02429947 Completed - Tooth Diseases Clinical Trials

An Analysis of the Symptomatic Domains Most Relevant to Charcot Marie Tooth Neuropathy (CMT) Patients

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to identify the issues that have greatest impact on QOL for patients with Charcot Marie Tooth (CMT) Disease. Patients who have -registered in the Inherited Neuropathies Consortium Contact Registry will be invited to participate.

NCT ID: NCT02425176 Completed - Sialorrhea Clinical Trials

Botulinum Toxin-A for Sialorrhoea Treatment in Asian Adults With Neurological Diseases

Start date: September 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The efficacy of Botulinum toxin A (BoNT-A) in Asian population has not been properly studied and there is no literature available on the most efficacious dose of BoNT-A for sialorrhoea treatment. This research is aimed to find the dose of Dysport® that would be efficacious without treatment-related adverse events and the duration of effectiveness of the drug for sialorrhea treatment in Malaysian patients. The efficacy, safety, tolerability and adverse effects of three doses of Dysport®(50MU, 100MU and 200MU) are examined at 2,6,12 and 24 weeks post injection in this double-blinding, randomized trial.

NCT ID: NCT02418286 Completed - Pain Clinical Trials

KLOS Study - Korean Medicine Registry for Low Back Pain Patients, a Prospective, Observational, Multicenter, Pilot Study

KLOS
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

The Purpose of this trial is to define the characteristics of the in/outpatients with low back pain in traditional Korean medicine rehabilitation clinic. This information will create a registry that will help us to compare similarities and differences in patients and their symptoms. The more patients the investigators are able to enter into the registry, the more the investigators will be able to understand the low back pain and learn better ways of caring for patients.

NCT ID: NCT02397681 Completed - Clinical trials for Autonomic Nervous System Diseases

Autonomic Responses During the Valsalva Maneuver and Deep Breathing Test Depend on the Experimental Setup

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of procedural differences during the Valsalva maneuver and deep breathing test in autonomic nervous system testing.

NCT ID: NCT02385877 Completed - Clinical trials for Autonomic Peripheral Nervous System Diseases

Clinical Translation of 18F-Labeled Hydroxyphenethylguanidines

Start date: March 2015
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to perform first-in-human PET imaging studies of two new cardiac sympathetic nerve imaging agents, 4-[18F]fluoro-meta-hydroxyphenethylguanidine ([18F]4F-MHPG) and 3-[18F]fluoro-para-hydroxyphenethylguanidine ([18F]3F-PHPG).

NCT ID: NCT02381977 Completed - Stroke Clinical Trials

Prevalence of Acute Critical Neurological Disease in Children: a Global Epidemiological Assessment

PANGEA
Start date: November 2011
Phase: N/A
Study type: Observational

PANGEA is an international prospective point prevalence study to describe the epidemiology, interventions, and outcomes in children with acute critical brain disease.