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Cerebral Infarction clinical trials

View clinical trials related to Cerebral Infarction.

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NCT ID: NCT01312623 Terminated - Cerebral Ischemia Clinical Trials

Organ Protection by Remote Ischemic Preconditioning for Surgical Treatment of Pediatric Congenital Heart Disease

RIPHeart
Start date: March 2010
Phase: N/A
Study type: Interventional

Cardiac surgery is associated with risk of perioperative inflammation and ischemia leading to cerebral and myocardial morbidity and mortality. Ischemic preconditioning by repetitive ischemic episodes at an organ can reduce damage resulting from consecutive prolonged ischemia in that organ. Remote ischemic preconditioning is defined as ischemic preconditioning by repetitive ischemic episodes of an organ remote from the organ to be protected, e.g. ischemic episodes of a limb can reduce ischemic damage of the heart. Animal studies as well as human studies have shown that ischemic preconditioning can protect the heart from intraoperative ischemia. Remote preconditioning by repetitive limb ischemia has been applied in humans in some studies.12-14 However, the published data is not yet sufficient to support evidence based recommendations for clinical practice. In particular, available data regarding the influence of remote preconditioning on inflammatory and ischemic damage of brain and heart in children following surgery of congenital heart disease are limited. Hence, this prospective, controlled and randomized study was designed to perform remote ischemic preconditioning in children after induction of anesthesia for pediatric heart surgery and to investigate the effect on postoperative organ function in comparison to a control group.

NCT ID: NCT00841633 Terminated - Clinical trials for Subarachnoid Hemorrhage

Induced Hypertension for Delayed Cerebral Ischaemia After Aneurysmal Subarachnoid Haemorrhage:a Feasibility Study

Start date: February 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the feasibility of a trial on induced hypertension to improve neurological outcome in patients with subarachnoid haemorrhage that developed the serious complication "delayed cerebral ischemia", and to assess whether induced hypertension results in improved cerebral blood flow (CBF) as measured by means of perfusion-CT.

NCT ID: NCT00414726 Terminated - Ischemic Stroke Clinical Trials

Normobaric Oxygen Therapy in Acute Ischemic Stroke Trial

Start date: January 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and efficacy of treating individuals with acute ischemic stroke with normobaric oxygen therapy (NBO, given within 9 hours of symptom onset), to standard medical treatment.

NCT ID: NCT00331890 Terminated - Acute Stroke Clinical Trials

ICTUS Study: International Citicoline Trial on Acute Stroke

ICTUS
Start date: October 2006
Phase: Phase 3
Study type: Interventional

Citicoline is a safe drug approved in some countries for the treatment of acute ischemic stroke. The drug has shown some evidence of efficacy in a pooled analysis, based on four clinical trials done in USA with oral citicoline.The purpose of the study is confirm the results obtained in the pooled analysis, that is, evidence of efficacy in the treatment of acute ischemic stroke

NCT ID: NCT00300196 Terminated - Stroke Clinical Trials

ASP-II: Ancrod Stroke Program: Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke

Start date: March 2006
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.

NCT ID: NCT00235495 Terminated - Ischemic Stroke Clinical Trials

Albumin in Acute Ischemic Stroke Trial

ALIAS
Start date: June 2006
Phase: Phase 3
Study type: Interventional

The goal of the trial is to determine whether human albumin, administered within 5 hours of symptom onset, improves the 3-month outcome of subjects with acute ischemic stroke.

NCT ID: NCT00141011 Terminated - Stroke Clinical Trials

Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke

Start date: September 2005
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.

NCT ID: NCT00029146 Terminated - Stroke Clinical Trials

Carotid Occlusion Surgery Study

COSS
Start date: July 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if extracranial-intracranial bypass surgery when added to best medical therapy can reduce the subsequent risk of ipsilateral stroke in high-risk patients with recently symptomatic carotid occlusion and increased cerebral oxygen extraction fraction measured by positron emission tomography (PET).

NCT ID: NCT00004728 Terminated - Stroke Clinical Trials

Aspirin Or Warfarin To Prevent Stroke

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether aspirin or warfarin is more effective in preventing stroke in patients with intracranial stenosis.