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Ischemic Stroke clinical trials

View clinical trials related to Ischemic Stroke.

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NCT ID: NCT02140658 Completed - Ischemic Stroke Clinical Trials

Affect of Health Education on Statins Medication Persistence and ClinicaL Prognosis of Ischemic Stroke Patients (HELP)

Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the affect of multiple health education interventions for statins medication Persistence and clinical prognosis of ischemic stroke patients at 3, 6 and 12 months.

NCT ID: NCT02140619 Completed - Ischemic Stroke Clinical Trials

Affect of Multiple Health Education on Medication Persistence and Clinical Prognosis of Ischemic Stroke Patients

Start date: May 2014
Phase: N/A
Study type: Interventional

The study aimed to demonstrate the relationship between secondary prevention medication persistence and clinical prognosis of ischemic stroke patients at 3,6,12 months

NCT ID: NCT02135926 Terminated - Ischemic Stroke Clinical Trials

Thrombectomy in Patients Ineligible for iv tPA

THRILL
Start date: March 2014
Phase: N/A
Study type: Interventional

the purpose of this study is to to compare the safety and effectiveness of stent-retrievers as a device class group with best medical care alone in the treatment of acute ischemic stroke (AIS) in patients who are not eligible for IV-tPA up to 8 hours of symptom onset.

NCT ID: NCT02133521 Terminated - Clinical trials for Acute Ischemic Stroke

DLBS1033 for Acute Ischemic Stroke Patients

ADDLIST
Start date: November 11, 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This is a prospective, randomized, double-blind, and controlled clinical study to investigate the effects of DLBS1033 in conjunction with standard therapy compared to standard therapy alone in acute ischemic stroke patients. It is hypothesized that the improvement in functional outcomes as measured by NIHSS and BI as well as the improvement in haemostatic parameters as measured by thrombocyte aggregation test (TAT), fibrinogen, and d-dimer in DLBS group will be significantly greater than those in the control group.

NCT ID: NCT02126982 Completed - Clinical trials for Coronary Artery Disease

Salts of Clopidogrel: Investigation to ENsure Clinical Equivalence

SCIENCE
Start date: October 2012
Phase:
Study type: Observational

Clopidogrel besylate (CB) is not differentiated relative to the orignal clopidogrel hydrogen sulfate (CHS) in the pharmacokinetics and in antiplatelet potency in healthy volunteers. In addition,CB exhibits similar pharmacodynamic properties compared to CHS in patients with a history of acute coronary syndrome (ACS) and in patients with ACS undergoing percutaneous coronary intervention (PCI). However, there is a lack of data on the clinical efficacy and safety of this salt to the original salt in patients with cardiovascular disease. The aim of this study is to investigate the clinical efficacy and safety of CB in relation to that of CHS in patients eligible to receive clopidogrel.

NCT ID: NCT02122718 Completed - Ischaemic Stroke Clinical Trials

XILO-FIST, the Effect of Allopurinol on the Brain Heart and Blood Pressure After Stroke

XILO-FIST
Start date: May 2014
Phase: Phase 4
Study type: Interventional

Recurrent stroke and cognitive decline are common after ischaemic stroke. Allopurinol, a drug usually used to treat gout, has been shown to reduce heart ischaemia, heart size, and arterial stiffness and to relax brain blood vessels and may reduce the blood pressure. All of these properties may be associated with a lower risk of second stroke and cognitive decline. We now aim to explore whether allopurinol will reduce further damage to the brain (called white matter hyper-intensities) after stroke and also whether it reduces heart size and blood pressure after stroke. We will conduct a multi-centre randomised, double-blind placebo controlled study to investigate whether two years allopurinol 300 mg twice per day (BD) improves these 3 outcomes, which are inextricably linked to risk of recurrence and cognitive decline after ischaemic stroke.

NCT ID: NCT02121327 Completed - Ischemic Stroke Clinical Trials

The Effects of Disease Management Programs for Prevention of Recurrent Ischemic Stroke

Start date: September 2010
Phase: N/A
Study type: Interventional

It has been reported that stroke is the first cause of becoming bedridden, and its cumulative recurrence rate in 5 years is approximately 35%. There is a high probability that patients reduce or discontinue medications by self-determination, leading to a high risk of stroke recurrence in these patients. Comprehensive and long-term patient educations ameliorating their self-management are important making patients possible to be managed according to the guidelines for their risk factors. Using disease management programs created for each of risk factors according to clinical practice guidelines, the influence of those programs were evaluated for the prevention of stroke recurrence in this Disease Management Program Stroke Trial.

NCT ID: NCT02090270 Completed - ISCHEMIC STROKE Clinical Trials

Hair Cortisol and the Risk of Stroke

Start date: March 2014
Phase: N/A
Study type: Observational

The purpose of this study is to prospectively examine the relation between ischemic stroke and hair cortisol concentration. The investigators hypothesize that patients with ischemic stroke have higher levels of hair cortisol compared to controls.

NCT ID: NCT02072681 Completed - Ischemic Stroke Clinical Trials

Mild and Rapidly Improving Stroke Study

MaRISS
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to determine the 90-day outcomes of mild and rapidly improving ischemic stroke.

NCT ID: NCT02062021 Active, not recruiting - Stroke Clinical Trials

Understanding the Role of Autoimmune Disorders on the Initial Presentation of Cardiovascular Disease

Start date: January 2014
Phase: N/A
Study type: Observational

Autoimmune diseases are diseases in which inappropriate immune responses that have the capability of harming host cells play an important role. Evidence suggests that the presence of certain autoimmune diseases such as rheumatoid arthritis or systematic lupus erythematosus increase the risk of cardiovascular disease (CVD). However, this evidence is inconsistent for autoimmune disorders and no systematic approach has been previously used to study the relationship between a range of common autoimmune disorders and specific forms of cardiovascular diseases such as myocardial infarction, intracerebral and subarachnoid haemorrhage, or venous thrombosis. The investigators will use linked electronic health records to investigate whether commonly diagnosed autoimmune disorders are associated with increased risk of CVD development and whether effects differ in men and women and change with age.