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Cerebral Hemorrhage clinical trials

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NCT ID: NCT01530880 Recruiting - Fever Clinical Trials

Aggressive Fever Control With Intravenous Ibuprofen After Non-traumatic Brain Hemorrhage

Start date: February 2012
Phase: Phase 4
Study type: Interventional

Fever, defined as temperature higher than 38.3C (100.9 F), is common in patients with head injuries and is associated with poor recovery after injury. The current standard of care is to use oral acetaminophen (Tylenol) followed by a body cooling device. This method can effectively reduce fever but results in a high rate of shivering. Shivering is stressful to the heart and can further worsen brain injury. Methods to combat shivering have been developed and are successful in limiting the stress in the majority of patients that use a body cooling device. However, the drugs used to control shivering are sedating and may also interfere with brain recovery. The purpose of this study is to assess whether ibuprofen given intravenously is more effective in combating fever than the current standard of care. Should results from this study demonstrate that ibuprofen infusion is effective, a larger study will be conducted to determine whether this aggressive fever control regimen leads to improved recovery after brain injury.

NCT ID: NCT01158807 Recruiting - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Cerebral Hemorrhage Risk in Hereditary Hemorrhagic Telangiectasia

BVMC6203
Start date: April 8, 2010
Phase:
Study type: Observational

This study is one of the three projects of an NIH Rare Disease Clinical Research Consortium. A "consortium" is a group of centres sharing information and resources to perform research. The consortium research focuses on brain blood vessel malformations in three different rare diseases. The focus of this specific study is on Hemorrhagic Telangiectasia (HHT). HHT is a condition characterized by blood vessel malformations, called telangiectasia and arteriovenous malformations (AVMs), occurring in the brain, nose, lungs, stomach, bowels and liver. Brain AVMs (BAVMs) in HHT are difficult to study because they are rare, affecting approximately 10% of people with HHT. While other types of BAVMs have been studied in depth, studies in the HHT population have been very small. Here, we propose the first large-scale collaboration by joining with 12 HHT Centers of Excellence in North America to perform a large study of risk factors for bleeding from BAVMs, called intracranial hemorrhage (ICH) in HHT patients. The current standard of clinical practice across North America, is to screen all HHT patients for BAVMs with magnetic resonance imaging (MRI). If BAVMs are detected, patients are referred to a multidisciplinary neurovascular team for consideration for treatment. Treatment decisions are made on a case by case basis, balancing risks of complications from the BAVM with risks of therapy, but are limited by the few studies available in HHT. We hope that the knowledge we obtain about the risk factors for intracranial bleeding in these patients from this larger study will help us to improve the care of HHT patients. We plan to study risk factors for rupture of BAVMs, including primarily genetics and imaging characteristics of the BAVMs. Knowledge about risk factors will help in the care and management of HHT patients. This will be achieved through the collection of health information to construct a HHT database, blood sampling and banking (through the National Institute of Neurological Disorders and Stroke [NINDS]), and through genetic analysis at the University of California San Francisco.

NCT ID: NCT01098890 Recruiting - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Intraventricular Tissue Plasminogen Activator (tPA) in the Management of Aneurysmal Subarachnoid Hemorrhage

Start date: October 2009
Phase: Phase 2
Study type: Interventional

The proposed study is to evaluate the acceleration the clearance of intraventricular blood (IVH) and subarachnoid hemorrhage (SAH) following ruptured intracranial aneurysms, thereby ameliorating complications, such as cerebral vasospasm, hydrocephalus and intracranial hypertension. The primary objectives are: 1. Estimate the rate and variance of hematoma clearance following aneurysmal SAH, thereby facilitating sample size determination for a subsequent larger study; 2. Assess the feasibility of a randomized controlled trial of intraventricular tissue plasminogen activator (TPA) among patients with SAH (enrollment rate, ability to blind investigators, protocol compliance); 3. Confirm the safety of intraventricular TPA.

NCT ID: NCT01064011 Recruiting - Clinical trials for Intraventricular Hemorrhage

Prospective Randomized, Controlled Trial for Treatment of Intraventricular Hemorrhage

IVH
Start date: January 2010
Phase: N/A
Study type: Interventional

Intraventricular hemorrhage comprises about 15% of the 500,000 strokes that occur annually in the United States. In the emergent setting, patients with obstructive hydrocephalus are routinely treated with placement of an external ventricular drain. This study will compare the effect of external ventricular drainage plus intraventricular thrombolysis versus external ventricular drainage plus endoscopic evacuation on neurologic outcomes for patients with hydrocephalus from intraventricular hemorrhage.

NCT ID: NCT00713375 Recruiting - Clinical trials for Subarachnoid Hemorrhage

Time Frequency Analysis of Electrocardiogram and Blood Pressure in Intracranial Hemorrhage Patients

Start date: April 2008
Phase: N/A
Study type: Observational

Dysregulation of autonomic nervous system is evident in patients with spontaneous intracranial hemorrhage. In this study, we utilize a non-invasive method (heart rate and blood pressure variability analysis to analyze the autonomic activities in this group of neurosurgical patients. Our aim is to determine the utility of this modality in risk stratification and outcome prediction in these patients.

NCT ID: NCT00699621 Recruiting - Clinical trials for Intracerebral Hemorrhage

Platelet Transfusion in Acute Intracerebral Hemorrhage

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

- To prove whether use of antiplatelet agents results into a rapid enlargement of hematoma after onset of acute intracerebral hemorrhage. - To prove the efficacy and safety of platelet transfusion for prevention of hematoma growth in patients who were stricken by acute intracerebral hemorrhage while being on antiplatelet medication.

NCT ID: NCT00699465 Recruiting - Clinical trials for Intracerebral Hemorrhage

Prevention of Venous Thromboembolism in Patients With Acute Primary Intracerebral Hemorrhage

Start date: August 2008
Phase: Phase 4
Study type: Interventional

- To evaluate the efficacy of using IPC during the acute phase of ICH in the prevention of VTE. - To assess the safety and efficacy of additional therapy with enoxaparin. - To compare the efficacy and safety of the European and American guideline recommendations. - To provide an efficient and safe thromboprophylaxis for several weeks until the patient is able to walk.

NCT ID: NCT00419874 Recruiting - Clinical trials for Traumatic Brain Injury

Characteristics of Blood- Brain Barrier Permeability in Neurological Patients

Start date: n/a
Phase: N/A
Study type: Observational

The main goal of the present study is to challenge the hypothesis that blood- brain barrier disruption following brain injury increases the risk for long-term disability, development of brain dysfunction, epileptic seizures and neuroanatomical alterations.

NCT ID: NCT00222625 Recruiting - Clinical trials for Intracerebral Hemorrhage

rFVIIa in ICH in Patients Treated With Anticoagulants or Anti-Platelets

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Evaluation of efficacy and safety of recombinant factor VIIa versus standard therapy in preventing early haematoma growth in spontaneous acute intracerebral haemorrhage in patients treated with oral anticoagulants or antiplatelets agents