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Cerebral Hemorrhage clinical trials

View clinical trials related to Cerebral Hemorrhage.

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NCT ID: NCT01417117 Completed - Ischemic Strokes Clinical Trials

Effect of Ischemic Strokes on Recovery From Intracerebral Hemorrhages

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

Intracerebral hemorrhage (ICH) occurs when small arteries in the brain rupture due to weakening by age, high blood pressure, and/or elevated cholesterol. In addition to artery rupture, recent data suggests that patients with ICH are also at risk for developing occlusion of arteries during the acute phase, called ischemic strokes. Data suggests these ischemic strokes can negatively impact patient outcomes. Diffusion weighted imaging (DWI) is a sequence on Magnetic Resonance Imaging (MRI) that is a sensitive marker for ischemic strokes in the brain. In this proposal, our primary aim is examine prospectively the effect DWI abnormalities have on functional outcomes in patients with ICH. Our hypothesis is that the DWI abnormalities found on MRI of the brain lead to worse functional outcomes in patients with ICH

NCT ID: NCT01409252 Completed - Stroke Clinical Trials

Long Term Outcome After Hemorrhagic Stroke Surgery

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

The investigators retrospectively reviewed all patients with neurosurgical operations for hemorrhagic stroke (intracerebral hemorrhage) between 1999 and 2008. Research assistant then telephoned the survivors for neurological and cognitive status.

NCT ID: NCT01359202 Completed - Stroke Clinical Trials

"Spot Sign" Selection of Intracerebral Hemorrhage to Guide Hemostatic Therapy

SPOTLIGHT
Start date: May 2011
Phase: Phase 2
Study type: Interventional

This clinical trial will enroll 110 patients from approximately 15 Canadian stroke centres. Patients coming to the emergency department with bleeding in the brain not due to trauma or other known causes who can be treated within 6 hours of onset will undergo CT angiography using standard CT scanners ("CAT scan"). Those with a "spot sign", a type of marker on the CT scan that shows the brain is still bleeding, will be randomly assigned to a single injection of "factor 7"(a blood clotting drug used in hemophilia) or placebo (inactive saline); patients without a spot sign will not be treated. The researchers will look at how much bleeding happens after the treatments are administered, as well as clinical outcomes such as death and disability. The researchers think that factor 7 will cause the bleeding to stop faster and possibly decrease death and disability.

NCT ID: NCT01261091 Completed - Ischemic Stroke Clinical Trials

Early Tracheostomy in Ventilated Stroke Patients

SETPOINT
Start date: September 2009
Phase: N/A
Study type: Interventional

Patients with severe ischemic and hemorrhagic strokes, who require mechanical ventilation, have a particularly bad prognosis. If they require long-term ventilation, their orotracheal tube needs to be, like in any other intensive care patient, replaced by a shorter tracheal tube below the larynx. This so called tracheostomy might be associated with advantages such as less demand of narcotics and pain killers, less lesions in mouth and larynx, better mouth hygiene, safer airway, more patient comfort and earlier mobilisation. The best timepoint for tracheostomy in stroke, however, is not known. This study investigates the potential benefits of early tracheostomy in ventilated critically ill patients with ischemic or hemorrhagic stroke.

NCT ID: NCT01202864 Completed - Clinical trials for Intracerebral Hemorrhage

Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH)

ERICH
Start date: August 1, 2010
Phase: N/A
Study type: Observational

The purpose of this study is to find risk factors for hemorrhagic stroke, specifically intracerebral hemorrhage (ICH), among Caucasians, African Americans, and Hispanics.

NCT ID: NCT01122212 Completed - Clinical trials for Intracerebral Hemorrhage

Introduction of Protein S100 in Diagnostics in Minor Brain Injury Patients at Our Hospital

S100
Start date: January 2010
Phase: N/A
Study type: Observational

In Patients with minor head injury measurement of protein S100 will be introduced to the emergency departement as another tool to rule out intracerebral bleeding.

NCT ID: NCT01115959 Completed - Clinical trials for Post Cerebral Hemorrhage

Seizures Post Intracerebral Hemorrhage

Start date: February 2003
Phase: Phase 4
Study type: Interventional

This study examines early antiepileptic treatment with valproic acid for acute cerebral hemorrhage against a placebo group immediately post event to evaluate the outcome of these patients regarding seizures and neurological outcome.

NCT ID: NCT01113645 Completed - Clinical trials for Infarction, Middle Cerebral Artery

Impact of Cranioplasty On Cerebral Perfusion

CCP
Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this study is to examine the impact of cranioplasty on cerebral hemodynamic and blood flow as prognostic factor in patients receiving decompressive craniectomy for Head injuries, Subarachnoid haemorrhage, intra-cerebral haemorrhage, cerebral dural sinus thrombosis, malignant middle cerebral artery stroke.

NCT ID: NCT01041950 Completed - Clinical trials for Intracerebral Hemorrhage

A Randomised Controlled Trial of Lumbar Drainage to Treat Communicating Hydrocephalus After Severe Intraventricular Hemorrhage

LUCAS-IVH
Start date: May 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if usage of early lumbar drainage leads to less shunt surgery and less catheter associated complications in patients with communicating hydrocephalus after intracerebral hemorrhage with severe ventricular involvement.

NCT ID: NCT00963976 Completed - Clinical trials for Intracerebral Hemorrhage

Intracerebral Hemorrhage Acutely Decreasing Arterial Pressure Trial

ICH ADAPT
Start date: January 2007
Phase: Phase 2
Study type: Interventional

Rationale: Management of blood pressure (BP) in the acute phase of intracerebral hemorrhage (ICH) remains controversial. Although it has been established that there is a transient moderate reduction of perihematoma cerebral blood flow (CBF) in acute ICH, the effect of BP treatment is unknown. The potential for exacerbation of CBF has precluded routine aggressive BP reduction. Aim and Hypothesis: The primary study aim is to demonstrate the feasibility and safety of acute BP reduction to < 150 mmHg systolic using a standardized protocol in ICH patients. It is hypothesized that CTP will not demonstrate evidence of perihematoma ischemia following acute BP reduction. Design: ICH ADAPT is a randomized blinded endpoint trial. Acutely hypertensive ICH patients are randomized to a target systolic BP of < 150 mmHg or < 180 mmHg. Patients are treated with intravenous (IV) labetalol/hydralazine/enalapril. Study Outcomes: The primary outcome is cerebral blood flow in the perihematoma region, measured with CT perfusion, 2 hours after randomization. Secondary outcomes include the difference in BP at 1 and 2 hours post-randomization in the two treatment groups and hematoma expansion rates at 24 hours. Discussion: ICH ADAPT is the only randomized trial designed specifically to identify any hemodynamic changes in the perihematoma region secondary to aggressive BP management. The results of this trial will facilitate ongoing and future studies aimed at determining the efficacy of rapid BP reduction in acute ICH.