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Encephalopathy clinical trials

View clinical trials related to Encephalopathy.

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NCT ID: NCT03173196 Completed - Encephalopathy Clinical Trials

Prospective Analysis of Septic Associated Encephalopathy Using the Non-invasive Acoustocerebrography-ACG

SAEACG
Start date: June 1, 2016
Phase: N/A
Study type: Observational

The patients of the group "sepsis" are measured several times with the non-invasive multi-spectral sonography (Sonovum "ACG-Diagnosesystem") (days 1, 3, 7 and 14). The patients of the group "control" are measured on days 1 and 3 with the system. A measurement takes 3 minutes. For this purpose two ultrasound heads are placed above the patient's ears and fixed with an all-head harness. The device is certified for CE application. There are no known health risks of ultrasound in humans.

NCT ID: NCT03138876 Completed - Encephalopathy Clinical Trials

EEG Cap for Identification of Non-Convulsive Status Epilepticus

Start date: May 30, 2017
Phase: N/A
Study type: Interventional

Altered mental status (AMS) is one of the most common reasons for inpatient neurology consultation. Non-convulsive status epilepticus (NCSE) is frequently on the differential diagnosis of the patient with AMS. NCSE becomes more refractory to treatment after one hour of seizure activity, making rapid identification and treatment of NCSE of great clinical importance. Currently, an electroencephalogram (EEG) technologist must be called in from home during non-workday hours in order to obtain a stat EEG. The investigators propose the time required for diagnosis of NCSE at Mayo Clinic can be significantly decreased with rapid placement of an EEG cap by the onsite neurology residents.

NCT ID: NCT02831010 Completed - Encephalopathy Clinical Trials

A Multi-Center Cohort Study of Risk Factors and Outcomes of Encephalopathy of Prematurity in China

Start date: April 2014
Phase:
Study type: Observational

The purpose of this study is to explore the perinatal risk factors of encephalopathy of prematurity and the morbidity of the following neurodevelopmental impairments in preterm infants with gestational age <32 weeks in China.

NCT ID: NCT02445417 Completed - Encephalopathy Clinical Trials

Brain Activity During Birth for Prediction of Newborns at Risk for Brain Injury

Start date: June 25, 2015
Phase:
Study type: Observational

The purpose of this study is early identification of asphyxiated newborns through eeg starting in the delivery room.

NCT ID: NCT01425385 Completed - Clinical trials for Liver Transplantation

Autoregulation Assessment During Liver Transplantation

Start date: September 2011
Phase: N/A
Study type: Observational

Patients with liver failure undergoing liver transplantation often have clinical or sub-clinical encephalopathy that may lead to increased intracranial pressure. The latter may lead to abnormal regulation of blood flow to the brain (cerebral autoregulation) complicating patient management during and after general anesthesia. The current methods for monitoring for elevated intracranial pressure are invasive and, thus, limited to severe encephalopathy. In this study the investigators will evaluate the potential utility of monitoring cerebral blood flow (CBF) autoregulation non-invasively using near infra-red spectroscopy in patients undergoing liver transplantation.

NCT ID: NCT01027715 Completed - Seizures Clinical Trials

The Impact of Electroencephalographic (EEG) Seizure Treatment in Neonatal Encephalopathy

Start date: January 2010
Phase: N/A
Study type: Interventional

This is a prospective, randomized, single-center pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG. The investigators hypothesize that the accurate detection and treatment of EEG seizures will decrease the seizure burden and improve outcomes in newborn infants with seizures and/or hypoxic-ischemic encephalopathy (HIE).

NCT ID: NCT00831337 Completed - Liver Cirrhosis Clinical Trials

Evaluation of Probiotics in the Treatment of Portal Hypertension

Start date: April 2007
Phase: N/A
Study type: Interventional

This study is to evaluate the role of probiotics in the treatment of portal hypertension. In particular the role of probiotics on gut microbiota in liver cirrhosis patients will be studied and compared with cytokines and other substances implicated in the pathogenesis of portal hypertension. The hypothesis whether probiotics may change the prognosis of patients with portal hypertension will be studied. The hypothesis whether probiotics may halt the pathologic cascade of events leading to various complications (e.g. hepato-renal syndrome, spontaneous bacterial peritonitis, bleeding varices) will be reviewed.

NCT ID: NCT00764049 Completed - Cirrhosis Clinical Trials

Single Pass Albumin Dialysis in Patients With Cirrhosis

DACAR
Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to determine whether a simplified device of albumin dialysis also has beneficial effects.

NCT ID: NCT00570973 Completed - Cirrhosis Clinical Trials

Band Ligation Versus Transjugular Intrahepatic Portosystemic Stent Shunt (TIPS) in Cirrhotics With Recurrent Variceal Bleeding Non Responding to Medical Therapy

ENDOvsTIPS
Start date: November 2004
Phase: Phase 4
Study type: Interventional

Patients with liver cirrhoses and recent history of variceal bleeding, with HVPG documented non response to medical therapy with non selective beta blockers +/- mononitrates or variceal rebleeding during adequate medical therapy will be randomized to undergo either multi-session endoscopic multi-band ligation and continuation of medication or TIPS placement. Best treatment for this group of cirrhotic patients is not known so far.

NCT ID: NCT00515359 Completed - Encephalopathy Clinical Trials

RCT for Intermittent Versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies

Start date: June 2007
Phase: N/A
Study type: Interventional

RCT for Intermittent versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies