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Cerebral Hemorrhage clinical trials

View clinical trials related to Cerebral Hemorrhage.

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NCT ID: NCT01472224 Completed - Stroke Clinical Trials

Volume Measurement and Progression Surveillance of Intracerebral Haemorrhage Using Transcranial Ultrasound

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

This study investigates the ability of ultrasound to measure the volume of a brain hemorrhage in the acute phase after hospital admission. It is known that approximately 30% of patients admitted with a brain hemorrhage will suffer from enlargement of the hematoma within the first hours after admission. In this study the investigators measure the volume of the hematoma every 30 minutes up to 6 hours after admission and every 2 hours between 6-12 hours.

NCT ID: NCT01467206 Completed - Cerebral Infarction Clinical Trials

Life After STroke - the LAST Study

LAST
Start date: November 2011
Phase: N/A
Study type: Interventional

The LAST study is a Norwegian multi site randomised controlled trial that intends to assess the effect of a long term follow up program after stroke. The program consists of a coordinating physiotherapist who will encourage and motivate included patients to perform at least 60 minutes of intensive motor training every week and 30 minutes of physical activity every day for 18 months after inclusion. The primary hypothesis is that patients receiving a long term follow up program after stroke will have better motor function at end of follow up than patients receiving standard care. A total of 390 home dwelling stroke patients living in the municipality of Trondheim, Asker and Bærum will be included at the out-patient clinic at St. Olavs Hospital or Bærum Hospital three months after their stroke. Included patients will be randomised to an intervention group receiving the long term follow up program or to a control group receiving standard care. Motor function, mental health and physical functioning in daily life will be assessed at inclusion and 18 months later. The LAST study is funded by the Norwegian Research Council, the Norwegian University of Science and Technology and the Central Norway Regional Health Authority and will conclude at the end of 2015.

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: NCT01320423 Active, not recruiting - Clinical trials for Intracerebral Haemorrhage

Surgical Trial in Lobar Intracerebral Haemorrhage

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

To establish whether a policy of earlier surgical evacuation of the haematoma in selected patients with spontaneous lobar ICH will improve outcome compared to a policy of initial conservative treatment. The trial will also help to better define the indications for early surgery. This will overcome two of the criticisms of STICH (timing was too late and sometimes location was too deep). The subgroup identified in STICH is clinically sensible and the hypothesis identified for STICH II is in line with current neurosurgical opinion.

NCT ID: NCT01298830 Terminated - Clinical trials for Intracerebral Hemorrhage (ICH)

GLP-1 CellBeads® for the Treatment of Stroke Patients With Space-occupying Intracerebral Hemorrhage

Start date: October 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to assess the safety of GLP-1 CellBeads® in patients with space-occupying intracerebral hemorrhage.

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: NCT01221142 Not yet recruiting - Hypothermia Clinical Trials

Pilot Study of Hypothermia for Intracerebral Hemorrhage in Croatia

Start date: January 2011
Phase: Phase 3
Study type: Interventional

In this pilot study the researchers will investigate efficacy of hypothermia in the early stage of treatment patients with primary intracerebral hemorrhage.

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.