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Subarachnoid Hemorrhage clinical trials

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NCT ID: NCT01593267 Active, not recruiting - Clinical trials for Ruptured Cerebral Aneurysm

Barrow Ruptured Aneurysm Trial

BRAT
Start date: November 2002
Phase: N/A
Study type: Interventional

With evolving endovascular technologies there is a growing debate centered on the relative safety and efficacy of the currently accepted alternatives for the treatment of ruptured cerebral aneurysms in the face of acute subarachnoid hemorrhage (SAH). The purpose of this study is to compare the safety and efficacy of microsurgical clipping and endovascular coiling of acutely ruptured cerebral aneurysms in a prospective, randomized fashion.

NCT ID: NCT01585311 Terminated - Tachycardia Clinical Trials

Impact of Tachycardia on Outcome After Subarachnoid Hemorrhage (SAH)

Start date: March 2008
Phase:
Study type: Observational

The purpose of this retrospective study is to test the hypothesis that uncontrolled tachycardia serves as a risk factor for adverse cardiovascular events and poor outcome after Subarachnoid Hemorrhage (SAH).

NCT ID: NCT01573507 Completed - Clinical trials for Traumatic Brain Injury

Lactate Therapy After Traumatic Brain Injury

LS_TCC
Start date: March 2012
Phase: N/A
Study type: Interventional

Background: Although glucose is essential to cerebral function, abundant experimental and clinical evidence demonstrates that endogenously released lactate, rather than glucose, is the preferential energy substrate for the brain in conditions of stress and acute injury. In patients with severe Traumatic Brain Injury (TBI) and aneurysmal subarachnoid hemorrhage (SAH) monitored with cerebral microdialysis and brain tissue oxygen (PbtO2), our preliminary data show that increased brain extracellular lactate is frequently observed. Our findings indicate that elevated brain lactate more often occurs in the absence of brain hypoxia/ischemia and is mainly the consequence of increased cerebral glycolysis, i.e. it occurs in association with high extracellular pyruvate. These data suggest that the primary source of elevated lactate is activated glycolysis and strongly support the concept that endogenously released lactate can be utilized by the injured human brain as energy substrate. They prompt further investigation to examine whether exogenous lactate supplementation can be a valuable neuroprotective strategy after TBI or SAH. Indeed, in animal models of brain injury, administration of exogenous lactate improves neuronal and cognitive recovery. Hypothesis: The investigators test the hypothesis that lactate therapy, administered during the acute phase of TBI or SAH, might exercise neuroprotective actions by restoring brain energetics and improving brain tissue PO2 and cerebral blood flow (CBF). Aim of the study: The aim of this single-center study is to examine the effect of sodium lactate infusion on cerebral extracellular metabolites, brain tissue PO2 and cerebral blood flow, measured with CT perfusion and transcranial doppler (TCD). Design: Prospective phase II interventional study examining the effect of a continuous 3-6 hours infusion of sodium lactate (20-40 µmol/kg/min), administered within 48 hours from TBI or SAH, on cerebral extracellular glucose, pyruvate, glutamate, glycerol, PbtO2 and CBF.

NCT ID: NCT01569100 Completed - SAH Clinical Trials

Atorvastatin After Aneurysmal Subarachnoid Hemorrhage

Start date: December 2005
Phase: N/A
Study type: Observational

The 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, known as statins, have recently been demonstrated to improve endothelial function. Additionally, numerous studies have shown statins as having antiinflammatory and cell-signaling effects together with a selective up-regulation of the eNOS activity. These findings are of potential benefit for the prevention of cerebral vasospasm after a aneurysmal subarachnoid hemorrhage. Indeed, one of the possible mechanisms for this vasospasm is the eNOS depletion or even increase of eNOS expression after the hemorrhage. The purpose of this study is to observe the immediate effect of statins after aneurysmal subarachnoid hemorrhage (aSAH) in cerebral vasospasm and outcome at one year.

NCT ID: NCT01567449 Unknown status - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Risk Factors for Aneurysm Rebleeding

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

The purpose of this study is to examine the risk factors for aneurysm rebleeding.

NCT ID: NCT01565590 Terminated - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Effects of Dexmedetomidine on Inflammatory Cytokines in Patients With Aneurysmal Subarachnoid Hemorrhage

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of this research is to compare patients with aneurysmal subarachnoid hemorrhage on dexmedetomidine compared to propofol to assess if one group has decreased inflammation. The investigators hypothesis is that the group assigned to receive dexmedetomidine will have a more profound decrease in markers of inflammation over time.

NCT ID: NCT01537263 Recruiting - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Ultrasound Perfusion Imaging After Aneurysmal Subarachnoid Hemorrhage

PSAB
Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine wether delayed cerebral ischemia can be predicted by ultrasound brain perfusion imaging in patients with aneurysmal subarachnoid hemorrhage (SAH).

NCT ID: NCT01516671 Active, not recruiting - Clinical trials for Subarachnoid Hemorrhage

Neuroinflammation and Bispectral Index After Subarachnoid Hemorrhage

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

Subarachnoid hemorrhage (SAH) is associated with a high mortality and frequently leads to severe disability in survivors caused by cerebral vasospasm and infarction. This study aims to elucidate the role of neuroinflammation (endocannabinoids and cortisol levels in cerebrospinal fluid) in the pathophysiology of cerebral vasospasm and the value of the bilateral bispectral index (BIS) for the early diagnosis of cerebral vasospasm.

NCT ID: NCT01516658 Completed - Clinical trials for Subarachnoid Hemorrhage

HYdrogel Coil Versus Bare Platinum Coil in Recanalization Imaging Data Study

HYBRID
Start date: June 2012
Phase: N/A
Study type: Interventional

HYBRID study is prospective randomized open label controlled multi center trial, to compare Hydrocoil and bare platinum coil for recanalization after endovascular treatment of intracranial aneurysms.

NCT ID: NCT01463878 Terminated - Clinical trials for Subarachnoid Hemorrhage

Enteral Nutrition and Glycemic Variability Neurological Intensive Care Unit Study

ANUS1014
Start date: November 2011
Phase: Phase 4
Study type: Interventional

Primary Objective: To determine the effects of a diabetes specific enteral formula compared to a standard formula supplemented with protein (isocaloric and isonitrogenous) on the mean blood glucose and glycemic variability in a homogenous group of critically ill patients in a neurological ICU. Blood glucose will be recorded every minute using a continuous blood glucose monitor. The primary end points will be the difference between the mean blood glucose levels and the glucose variability between the control and intervention groups for the time period that the patient is in the ICU and receiving tube feeds and for up to a maximum of 14 days. Secondary Objectives: To determine the effects of the diabetes specific versus standard tube feeds on the change in muscle thickness and volume measured by 2-dimensional ultrasound imaging during the patients ICU stay.