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Stroke, Acute clinical trials

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NCT ID: NCT01585597 Completed - Stroke, Acute Clinical Trials

Reperfusion With Cooling in Cerebral Acute Ischemia

ReCCLAIM
Start date: May 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether reducing a patients body temperature (mild hypothermia of 33 degrees Centigrade) will significantly reduce the risk of brain injury (notably reperfusion injury and hemorrhagic conversion) in patients that have suffered a significant interruption of blood flow to an area of brain (occlusion of large proximal cerebral artery) and have undergone successful removal of that interruption (revascularization).

NCT ID: NCT01311544 Completed - Stroke, Acute Clinical Trials

Evaluation of 4D Magnetic Resonance Angiography (K-t Blast) of Supraortic Vessels in Acute Ischemic Stroke Patients

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

The Magnetic Resonance angiography (MRA) of supraaortic vessels is essential for the etiologic of stroke. However, the techniques usually used provide only static evaluation (degree of stenosis, occlusion) but not dynamic. An ultra-fast 3D MRA originally developed for the cardiac imaging, k-t blast (Broad-use Linear Acquisition Speed-up Technique) could be used to review the supraaortic vessels. This MRA offers the following advantages: short acquisition time, wide spatial coverage (of the thoracic aorta to the distal encephalic arteries), 3D spatial resolution and high temporal resolution. These qualities are even more optimal with a high magnetic field (3T). The high temporal resolution is interesting because it provides to repeat a volume every eight seconds and thus to have a dynamic evaluation of vascular filling and to assess the vascular supply of the infarcted territory. This sequence is classified as a 4D MRA.

NCT ID: NCT01182818 Completed - Stroke, Acute Clinical Trials

Fabry and Stroke Epidemiological Protocol (FASEP): Risk Factors In Ischemic Stroke Patients With Fabry Disease

FASEP
Start date: September 2010
Phase: N/A
Study type: Observational

More than one million people in Europe suffer from a stroke every day. Normally older people have a stroke, but also a significant number of younger people between 18 and 55 years. Usually, these can only be explained for a minority by the classical risk factors such as diabetes, overweight and high blood pressure. New studies indicate that in about 1 - 2 % of the younger stroke patients the etiology can be an undiagnosed genetic disease, e.g. Fabry disease. Fabry disease is a lysosomal storage disorder known to cause vasculopathy. The purpose of this study is to determine in a large number of young stroke patients, how many strokes were caused by Fabry disease and what risk factors might be able to predict this disease.

NCT ID: NCT01073007 Completed - Stroke, Acute Clinical Trials

Stroke Treatment With Acute Reperfusion and Simvastatin

Start date: April 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether simvastatin treatment started within the first 12 hours from stroke onset improves neurological and functional outcomes, evaluated at seventh day/discharge or at the third month. Also, to demonstrate that simvastatin is safe and not associated with higher rates of hemorrhagic transformation in patients who receive thrombolysis.

NCT ID: NCT00761982 Completed - Stroke, Acute Clinical Trials

Autologous Bone Marrow Stem Cells in Middle Cerebral Artery Acute Stroke Treatment.

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

The aim of the study is to determine the safety and efficacy on an autologous CD34+ subset bone marrow stem cell infusion into the middle cerebral artery in patients who have suffered acute middle cerebral artery stroke.

NCT ID: NCT00630396 Completed - Stroke, Acute Clinical Trials

Study of a Neuroprotective Drug to Limit the Extent of Damage From an Ischemic Stroke

MINOS
Start date: May 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The primary aim of this study is to find out which of 4 different doses of minocycline are safe and well tolerated so that we will know the optimal dose to test in future patients.

NCT ID: NCT00623350 Completed - Stroke, Acute Clinical Trials

Stroke DOC Arizona TIME - Stroke Team Remote Evaluation Using a Digital Observation Camera

Start date: December 2007
Phase: N/A
Study type: Interventional

Noninvasive prospective multi-center study of an interactive 2-way, wireless or site-independent, audiovisual telemedicine system designed for real-time remote examination of acute stroke symptoms and deficits as a basis for treatment consultation and recommendation. Study aims (1) to determine the impact of a site-independent, remote, telemedicine consultation system on decision making in the Emergency Department, regarding the decision to treat or not to treat with thrombolytics; (2) to assess the numbers of patients who receive thrombolytics and the time to treatment in patients evaluated by telemedicine versus telephone only; (3) to assess the appropriateness of thrombolytic treatment decisions in telemedicine versus telephone-only consultations; and (4) to assess the completeness of the data collection in telemedicine versus telephone-only consultations. 60 patients in Arizona with acute presentation of stroke symptoms, per bedside practitioner discretion (onset generally less than 12 hours and likely less than 3 hours) Two arms: Video Camera/Telemedicine (Intervention n = 30) and No Video Camera/Telephone only (Control n = 30)

NCT ID: NCT00604630 Completed - Stroke, Acute Clinical Trials

Multicenter Efficacy Study of Recombinant Human Erythropoietin in Acute Ischemic Stroke

ESS
Start date: January 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this randomized, double-blind, placebo-controlled multicenter study is to determine in a cohort of 506 patients with acute ischemic stroke in the middle cerebral artery territory, the effect of a three-day high-dose, intravenous erythropoietin treatment on functional outcome up to a follow-up of 90 days.

NCT ID: NCT00565045 Completed - Stroke Clinical Trials

Treatments for Recovery of Hand Function in Acute Stroke Survivors

Start date: July 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Impaired hand function is one of the most frequently persisting consequences of stroke. The purpose of this study is to investigate whether two different types of treatment improve recovery of hand function after stroke.

NCT ID: NCT00535197 Completed - Stroke, Acute Clinical Trials

Autologous Bone Marrow Stem Cells in Ischemic Stroke.

Start date: September 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to determine the safety and tolerability of an autologous CD34+ subset bone marrow stem cell infusion into the middle cerebral artery in patients who have suffered acute total or partial anterior circulation syndrome (TACS/PACS).