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Intracranial Hemorrhages clinical trials

View clinical trials related to Intracranial Hemorrhages.

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NCT ID: NCT01069250 Completed - Clinical trials for Intracranial Hemorrhages

Dynamic and Static Autoregulation After Brain Injury

Start date: August 2001
Phase: N/A
Study type: Observational

The aim of the study assesses static and dynamic cerebrovascular autoregulation daily over one week in patients with traumatic brain injury or intracranial hemorrhage to quantify the temporal profile of the autoregulatory status.

NCT ID: NCT00928915 Completed - Clinical trials for Intracranial Hemorrhages

International Normalized Ratio (INR) Normalization in Coumadin Associated Intracerebral Haemorrhage

INCH
Start date: July 2009
Phase: Phase 4
Study type: Interventional

Intracerebral haemorrhage (ICH) is the most feared complication in patients on vitamin K antagonists (VKA). VKA related ICH occurs 8-10 times more frequently and the mortality is 2 times higher than in non-anticoagulated patients. Mortality may rise up to 67%. The higher mortality rate may in part be due to the higher rate of haematoma expansion (HE) over a longer period after symptom onset. International guidelines recommend treatment of VKA-ICH with prothrombin complex (PCC) or fresh-frozen plasma (FFP) both in combination with Vitamin-K. But these recommendations are not based on randomized controlled trials. It is known that these drugs lower the INR, and thus it is assumed that normalization of coagulopathy may lead to haemostasis and reduction of HE. Safety and efficacy of these treatments have never been studied in a prospective controlled trial. The investigators' questions are: How potent are PCC and FFP in normalization of the INR? What is the safety profile of each of these drugs?

NCT ID: NCT00817310 Completed - Prematurity Clinical Trials

Neurophysiology and Anatomy of Severe Intraventricular Hemorrhage (IVH)

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

Currently, when premature infants develop severe intraventricular hemorrhage (IVH), a type of intracerebral bleed, there are no proven therapeutic interventions to prevent the devastating consequences of this event. These children will be likely to develop cerebral palsy or severe cognitive delays. The purpose of our study is to characterize differences in brain physiology, imaging, and function between premature infants with severe IVH and controls. The goals for gathering this information are to generate baseline data, which could facilitate early screening for complications of IVH in premature infants. These baseline data would also allow the design and implementation of early therapeutic interventions to help rehabilitate premature infants with severe IVH.

NCT ID: NCT00795119 Completed - Clinical trials for Intracranial Hemorrhage

A Trial to Determine the Efficacy of Near Infrared Spectroscopy to Detect Intracranial Hemorrhage in Children

NIRS
Start date: September 2007
Phase: N/A
Study type: Interventional

To diagnose bleeding inside the head, children need to have a CT Scan or MRI of their heads. Not all doctors order these though, especially when there is no history of injury or when children don't look too sick. Unfortunately, this means that some children's bleeding doesn't get diagnosed as early as it could. This study wants to find a way to detect bleeding inside the head without using a CT scan or MRI.

NCT ID: NCT00755209 Completed - Brain Injuries Clinical Trials

Tranexamic Acid for Preventing Progressive Intracranial Haemorrhage in Traumatic Brain Injury

Start date: October 2008
Phase: Phase 3
Study type: Interventional

The study's objective is to evaluate the effectiveness and safety of tranexamic acid for adult patients with moderate to severe TBI.With the research question as "Does TXA reduce the incidence of progressive intracranial haemorrhage by 50% compared to placebo in moderate to severe adult TBI patients at Khon Kaen Hospital?"

NCT ID: NCT00451789 Completed - Clinical trials for Traumatic Brain Injury

Risk Factors of Minor Head Injury

Start date: December 2004
Phase: N/A
Study type: Observational

Introduction and Aims: The objective of this prospective study is to evaluate the risk factors of minor head injury in all consecutive patients of one year.

NCT ID: NCT00413946 Completed - Cerebral Palsy Clinical Trials

Does Erythropoietin Improve Outcome in Very Preterm Infants?

Start date: January 2006
Phase: Phase 2
Study type: Interventional

The main goal of this trial is to investigate whether early administration of human erythropoietin (EPO) in very preterm infants improves neurodevelopmental outcome at 24 months corrected age. This study is designed as randomized, double-masked, placebo controlled multicenter study involving at least 420 patients.

NCT ID: NCT00369005 Completed - Anemia Clinical Trials

Liberal Versus Restrictive Transfusion Guidelines for Preterm Infants

Start date: December 1992
Phase: N/A
Study type: Interventional

The purpose of this study was to determine whether restrictive guidelines for red blood cell (RBC) transfusions for preterm infants can reduce the number of transfusions without adverse consequences.

NCT ID: NCT00226096 Completed - Clinical trials for Intracranial Hemorrhages

Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage

Start date: November 2005
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether lowering high blood pressure levels after the start of a stroke caused by bleeding in the brain (intracerebral haemorrhage) will reduce the chances of a person dying or surviving with a long term disability. The study will be undertaken in two phases: a vanguard phase in 400 patients, to plan for a main phase in 2000 patients.

NCT ID: NCT00120588 Completed - Preterm Birth Clinical Trials

Neuroprotection by Magnesium Sulfate Given to Women at Risk of Very Preterm Birth

Start date: July 1997
Phase: Phase 4
Study type: Interventional

Magnesium is neuroprotective in neonatal animal models of acquired hypoxic-ischemic and/or inflammatory cerebral lesions. It is associated with a significant reduction of perinatal death and cerebral palsy in some observational studies. The objective of the study is to assess if prenatal magnesium sulfate given to women at risk of preterm birth before 33 week's gestation is neuroprotective.