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Guillain-Barre Syndrome clinical trials

View clinical trials related to Guillain-Barre Syndrome.

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NCT ID: NCT01024088 Completed - Respiratory Failure Clinical Trials

Prospective Study on Swallowing/Breathing Interactions in Severe Guillain Barre Syndrome.

DGVSB
Start date: March 2008
Phase: N/A
Study type: Observational

To estimate, in a longitudinal and not invasive way, in patients with SGB at respiratory risk, the function of respiratory muscles and that of the upper airways muscles by investigating the force of the tongue, the gulp, and the breath during the sleep to be able to detect bulbar impairment and establish correlations enter the various parameters to estimate better the interactions between the dysfunction of the respiratory muscles and that upper airways muscles and so determine the risk acute respiratory failure.

NCT ID: NCT01005524 Completed - Tetraplegia Clinical Trials

Brain Computer Interface for Communication in ICU: a Feasibility Study

RoBIK-1
Start date: January 2010
Phase: N/A
Study type: Observational

The main objective of this study is to evaluate the usability of a system to assist verbal communication based on BCI system using the P300 wave in patients with tetraplegia who can no longer communicate because of severe engine damage (tetraplegia) and respiratory damage requiring invasive mechanical ventilation (intubation or tracheostomy) preventing verbal communication.

NCT ID: NCT00575653 Completed - Clinical trials for Guillain-Barre Syndrome

Safety Study of GBS Following Menactra Meningococcal Vaccination

Start date: March 2005
Phase: N/A
Study type: Observational

We are conducting a large, record-based study to assess the risk of Guillain-Barré Syndrome (GBS), a serious demyelinating disease, following immunization with the tetravalent meningococcal conjugate vaccine (Menactra) that is currently recommended for all adolescents. The study was requested by CDC and FDA because of an unexpected number of case reports to the CDC's Vaccine Adverse Event Reporting System (VAERS). The study protocol was designed by the investigators, with input from FDA, CDC, and the vaccine's manufacturer, Sanofi-Pasteur. An external advisory board that includes CDC representation, provides input regarding important decisions. The manufacturer is not participating in the conduct of the study and has no control over the analysis or dissemination of results. The study is derived from five large US health plans with a total membership of approximately 50 million over the study time period. America's Health Insurance Plans (AHIP) serves as liaison between the health plans and the Coordinating Center at the Department of Ambulatory Care and Prevention of Harvard Medical School and Harvard Pilgrim Health Care, and is the contracting organization with the health plans.

NCT ID: NCT00167622 Completed - Clinical trials for Acute Respiratory Failure

Early Mechanical Ventilation for Guillain Barré Syndrome

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

The purpose of this study is to determine whether early mechanical ventilation can prevent hospital acquired pneumonia in adults with Guillain Barré Syndrome.

NCT ID: NCT00056810 Completed - Clinical trials for Guillain-Barre Syndrome

Assessment of Chronic Guillain-Barre Syndrome Improvement With Use of 4-aminopyridine

Start date: September 2002
Phase: Phase 2
Study type: Interventional

In developed countries, Guillain-Barre Syndrome (GBS) is the most common cause of acute neuromuscular paralysis, afflicting about 5,000 persons annually in the United States. Over 20% of GBS patients have permanent residual motor deficits that affect their activities of daily living. The goal of this study is to assess the potential usefulness and safety of 4-aminopyridine (4-AP) in those patients who suffer chronic functional deficits from GBS.This medication is a potassium channel blocker that has the potential to improve nerve conduction, particularly across partially demyelinated axons. It is felt that by increasing nerve conduction there will be improved motor performance for walking and activities of daily living, as well as decreased fatiguability. This medication has demonstrated potential usefulness in central demyelinating diseases such as multiple sclerosis.Because the peripheral nervous system is much more accessible to systemic medication delivery it is felt that this medication may improve the functional status of those patients who are suffering from the residual side effects of this medication.