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Intracranial Hypertension clinical trials

View clinical trials related to Intracranial Hypertension.

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NCT ID: NCT01850069 Completed - Clinical trials for Intracranial Hypertension

The Use of Near Infrared Spectroscopy (NIRS) to Estimate Intracranial Pressure (ICP)

Start date: June 2014
Phase:
Study type: Observational

The aim of this study is to determine whether we can predict the intracranial pressure using near infra-red spectroscopy

NCT ID: NCT01796015 Completed - Cerebral Stroke Clinical Trials

Intracranial Hypertension and Optic Nerve Sheath Diameter

DENO
Start date: April 2011
Phase: N/A
Study type: Interventional

Intracranial hypertension (ICH) is a mortality risk factor in severe traumatic brain injury (TBI), in purulent meningitis, in hepatic encephalopathy and in Reye's syndrome. It is also a risk factor for severe neurologic sequelae in survivors. Intracranial pressure (ICP) monitoring is likely to guide therapeutics, and certain research on adults or on children, suggest that IH therapeutic approach, for instance for bacterial meningitis, would improve the prognosis. Two monitoring techniques are currently recommended. They are reference methods for ICP measure : - monitoring with intraventricular catheter, - intra-parenchymal monitoring using optical fiber catheter. Non invasive methods have been suggested, including ultrasound measurement of optic nerve sheath diameter (ONSD) which is the most interesting one. The ONSD measured ultrasonically is correlated with ICP level in adults with severe TBI. A diameter over 5,9 mm predicts ICH within the first 24 hours. In children, ONSD average values have been worked out, and an ONSD increase is found in children suffering from hydrocephalus with IH and in children with TBI. ICH precocious detection is fundamental in children sensitive to ICH because their cerebral development is not finished yet. Difficulties met for ICP monitoring implementation in infants and its invasive nature are often disliked by clinicians. A non-invasive exam is then essential to allow a better care of children with ICH in intensive care unit.

NCT ID: NCT01776801 Completed - Clinical trials for Increased Intracranial Pressure Disorders

Assessment of Autonomic Neuronal Changes During Moderate Rise of Intracranial Pressure in Human

CESNA
Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this project is to determine during moderate rise of intracranial pressure (ICP) in awake patient, the change in autonomic function and its influence on cerebral and systemic haemodynamics.

NCT ID: NCT01448681 Completed - Clinical trials for Intracranial Hypertension

A Continuous, Non-Invasive, Real-time Method for Estimating and Predicting Intracranial Hypertension

Start date: August 2011
Phase:
Study type: Observational

There is statistically significant correlation between invasive measures of intracranial pressure (ICP) and non-invasive, real-time, continuous physiologic waveform data algorithms to predict ICP. Furthermore, characteristics within this physiologic waveform data will allow modeling for trend prediction of derived ICP information. Specific aims: 1. Develop models to estimate ICP and cerebral perfusion pressure (CPP) after traumatic brain injury in humans. 2. Predict and anticipate changes in ICP for preemptive management purposes. 3. Analyze characteristics of changes in ICP after treatment failure. 4. Analyze data to predict/anticipate confounding physiologic factors that affect ICP and its treatment. 5. Test the resulting models in real time.

NCT ID: NCT01407809 Completed - Clinical trials for Idiopathic Intracranial Hypertension (IIH)

Venous Sinus Stenting for Idiopathic Intracranial Hypertension Refractory to Medical Therapy

VSSIIH
Start date: January 2012
Phase: Phase 1
Study type: Interventional

Idiopathic Intracranial Hypertension (IIH) is a disease that affects mainly young people, and is associated with headache and loss of vision. The medical and surgical management of IIH is problematic and many patients are not treated effectively. Some cases of IIH are associated with severe stenosis of the large veins of the brain and various researchers have recently reported significant improvement in patients with IIH after the narrow veins of the brain were treated with a stent. Our project aims to evaluate the safety and long-term efficacy of venous sinus stenting in patients with severe IIH refractory to medical management.

NCT ID: NCT01003639 Completed - Clinical trials for Idiopathic Intracranial Hypertension

Idiopathic Intracranial Hypertension Treatment Trial

IIHTT
Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Idiopathic intracranial hypertension (IIH), also called pseudotumor cerebri, is a disorder of elevated intracranial pressure of unknown cause [Corbett, et al., 1982; Wall, et al., 1991]. Its incidence is 22.5 new cases each year per 100,000 overweight women of childbearing age, and is rising [Garrett, et al., 2004] in parallel with the obesity epidemic. It affects about 100,000 Americans. Most patients suffer debilitating headaches. Because of pressure on the optic nerve (papilledema), 86% have some degree of permanent visual loss and 10% develop severe visual loss [Wall, et al., 1991]. Interventions to prevent loss of sight, all with unproven efficacy, include diet, diuretics such as acetazolamide, repeated spinal taps, optic nerve sheath fenestration surgery, and cerebrospinal fluid (CSF) shunting procedures. The purported goal of these therapies is to lower intracranial pressure; however, it is unclear which treatments work and by what mechanism. None of these strategies has been verified by properly designed clinical trials. Thus, there is confusion, uncertainty, and weak scientific rationales to guide treatment decisions. This trial will study subjects who have mild visual loss from IIH to (1) establish convincing, evidence-based treatment strategies for IIH to restore and protect vision, (2) follow subjects up to 4 years to observe the long-term treatment outcomes and (3) determine the cause of IIH. To meet those aims, the trial will be divided into a 12-month intervention phase and a 3-year observational phase. Subjects are not required to complete the observational phase of the study, but will be asked to do so and consented for the observational phase of the study at the conclusion of the intervention phase (12 months).

NCT ID: NCT00995683 Completed - Head Trauma Clinical Trials

Preventive Sodium Lactate and Traumatic Brain Injury

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

The goal of this study is to evaluate the effect of preventive intravenous infusion of half molar sodium lactate on the onset of hypertensive intracranial episodes in severe head trauma. The investigators hypothesize that preventive intravenous administration of sodium lactate will decrease the number of treatments required to decrease intracranial pressure during 48 hours.

NCT ID: NCT00670124 Completed - Clinical trials for Intracranial Hypertension

Hypothermia to Prevent High Intracranial Pressure in Patients With Acute Liver Failure

Start date: January 2005
Phase: N/A
Study type: Interventional

Treatment options in patients with high intracranial pressure due to acute liver failure are limited. This study intends to evaluate the effect of prophylactic hypothermia on preventing high intracranial pressure and compromised cerebral oxidative metabolism.

NCT ID: NCT00655304 Completed - Clinical trials for Hepatic Encephalopathy

The Effect of Prometheus (R) Liver Support Dialysis on Cerebral Metabolism in Acute Liver Failure

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

The main objective of this study is to investigate the effect of Prometheus liver support dialysis on intracranial pressure, cerebral metabolism and circulation in patients with acute liver failure.

NCT ID: NCT00571623 Completed - Brain Injury Clinical Trials

Automated Chest Physiotherapy to Improve Outcomes in Neuro

ACTION-ICP
Start date: September 2007
Phase: N/A
Study type: Observational

Following current standard-of-care, subjects data (brain pressure) will be recorded for 1 hour and include 10-minutes of data during which the subject recieves chest physiotherapy (CPT). The hypothesis is that CPT is not harmful to brain pressure.