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Brain Ischemia clinical trials

View clinical trials related to Brain Ischemia.

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NCT ID: NCT02455830 Active, not recruiting - Clinical trials for Neonatal Encephalopathy (Neonatal Hypoxic-ischemic Encephalopathy)

Cytokines Associated With Cord Blood Cell Therapy for Neonatal Encephalopathy

Start date: April 2015
Phase:
Study type: Observational

This is a observational study to assess the effects of and to explore the mechanisms of autologous umbilical cord blood cell therapy for neonatal encephalopathy by way of measuring serum cytokines.

NCT ID: NCT02056769 Active, not recruiting - Clinical trials for Subarachnoid Hemorrhage

CT Perfusion Imaging to Predict Vasospasm in Subarachnoid Hemorrhage

CT-PIPS
Start date: April 2014
Phase: N/A
Study type: Interventional

Patients with brain hemorrhage resulting from a ruptured aneurysm (SAH) are at risk of developing a condition called vasospasm, one or two weeks after their hemorrhage. This is a major cause of stroke and death following SAH. A special type of CT scan, called CT perfusion, analyzes regional blood flow in the brain. We hypothesize that CT perfusion scans performed on admission and day 6 post-hemorrhage will enable us to predict which patients will go on to develop vasospasm.

NCT ID: NCT01138176 Active, not recruiting - Clinical trials for Hypoxic Ischemic Encephalopathy

Whole Body Cooling Using Phase Changing Material

Start date: July 2009
Phase: Phase 1/Phase 2
Study type: Interventional

A prospective randomized control trial to examine safety and effectiveness of whole body cooling to a rectal temperature of 33.5 C using phase changing material in neonatal encephalopathy. Effectiveness will be defined by examining the stability of rectal temperature during cooling. Monitoring of vital signs, infection screen, blood counts, coagulation screen, liver and renal function tests, cranial US and MR imaging will be performed on recruited infants to evaluate safety of cooling. EEG will be performed on day 4 and hearing evaluation at discharge. Neurodevelopmental evaluation will be performed at 1 year of age.

NCT ID: NCT01104311 Active, not recruiting - Brain Ischemia Clinical Trials

Strategy for Adequate Blood Pressure Lowering in the Patients With Intracranial Atherosclerosis

STABLE-ICAS
Start date: April 2010
Phase: Phase 4
Study type: Interventional

To develop adequate blood pressure (BP) lowering strategy after subacute ischemic stroke patients with symptomatic severe intracranial atherosclerosis. Primary hypothesis of this study is that aggressive BP control (lowering systolic BP between 110mmHg and 120mmHg) will not increase the ischemic lesion volumes in hemisphere compared to modest BP lowering (lowering systolic BP between 130mmHg and 140mmHg) in the patients with symptomatic severe intracranial atherosclerosis.

NCT ID: NCT01013532 Active, not recruiting - Brain Ischemia Clinical Trials

PreventIon of CArdiovascular Events in iSchemic Stroke Patients With High Risk of Cerebral HemOrrhage

PICASSO
Start date: June 2009
Phase: Phase 4
Study type: Interventional

Through this study, the investigators are to prove that Cilostazol effectively prevent cardiovascular events in ischemic stroke patients with high risk of cerebral hemorrhage, along with no significant increase in the risk of occurrence of hemorrhagic side effects. The primary hypothesis of this study is; Cilostazol alone or with probucol will reduce the risk of cerebral hemorrhage without increase of cardiovascular events compared to aspirin in the ischemic stroke patients with symptomatic or asymptomatic old cerebral hemorrhage. This study will prove the superiority of cilostazol on the prevention of cerebral hemorrhagic events without increasing the cardiovascular events against aspirin and the superiority of probucol on the prevention of overall cardiovascular events.