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Stroke clinical trials

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NCT ID: NCT02481323 Completed - Stroke Clinical Trials

Lacunar Intervention Trial 1 (LACI-1)

Prevent-SVD
Start date: March 2016
Phase: Phase 2
Study type: Interventional

Phase II pilot randomised, factorial, short term dose escalation, open label, blinded intermediary endpoint trial, in two hospital centres in the UK, of tolerability and safety of cilostazol, isosorbide mononitrate, both or neither in patients with small vessel disease manifest as symptomatic small subcortical stroke.

NCT ID: NCT02481011 Completed - Stroke Clinical Trials

Risk of Intracranial Hemorrhage in Users of Oral Antithrombotic Drugs

RICH
Start date: May 2015
Phase:
Study type: Observational

The true incidence and risks of intracranial hemorrhage (ICH) in patients on various antithrombotic treatments remain unknown. Here a nationwide study is conducted to investigate the risk for and incidence rates of ICH in users and non-users of various oral antithrombotic drugs in Norway between 2008 through 2014. Hopefully, this study will contribute to a more responsible prescription pattern of antithrombotic medications.

NCT ID: NCT02480140 Completed - Stroke Clinical Trials

Self-regulated Constraint-induced Movement Therapy in Subacute Stroke Patients

Start date: September 2008
Phase: N/A
Study type: Interventional

Emerging research suggests the use of self-regulation (SR) strategies at improving functional regain in patients with brain injury. SR is proposed to produce an added effect to the effective constraint-induced movement therapy (CIMT). This study aimed to examine the efficacy of a self-regulated CIMT program (SR-CIMT) for function regain of patients with subacute stroke. It was hypothesized that participants receiving the combined treatment (SR and CIMT) would have a better functional regain.

NCT ID: NCT02479243 Recruiting - Stroke Clinical Trials

Assessment and Quantification of Collateral by ASL MRI

Start date: January 2014
Phase: N/A
Study type: Observational [Patient Registry]

Collateral circulation supports brain tissues to maintain blood perfusion in cerebral ischemic stroke and are of great benefit for a better outcome. A non-invasive approach relative to currently widely used digital subtraction angiography (DSA) is needed. ASL (arterial spin labeling) is a novel perfusion method without contrast agent injection and features both temporal and cerebral blood flow(CBF) information. The investigators applied multiple post labeled delay(PLD) time to pseudo-continuous Arterial Spin Labeling (3D pCASL) MRI and subtraction images were obtained to evaluate the collateral robustness and quantitatively assess the collateral perfusion in patients with unilateral middle cerebral artery atherosclerotic stenosis and the ability to predict future stroke recurrence.

NCT ID: NCT02478294 Completed - Stroke Clinical Trials

LAA Excision With AF Ablation Versus Oral Anticoagulants for Secondary Prevention of Stroke

5A
Start date: January 2013
Phase:
Study type: Observational

This cohort study aims to evaluate thoracoscopic left atrial appendage excision plus atrial fibrillation ablation versus oral anticoagulants for the prevention of stroke and non-central nervous systemic embolism in patients with atrial fibrillation and thromboembolism.

NCT ID: NCT02478177 Completed - Stroke Clinical Trials

Addressing Real-world Anticoagulant Management Issues in Stroke

ARAMIS
Start date: September 2015
Phase:
Study type: Observational [Patient Registry]

The Addressing Real-world Anticoagulant Management Issues in Stroke (ARAMIS) registry is designed to provide important and timely insight into the management of acute stroke patients who are on novel oral anticoagulants in community practice.

NCT ID: NCT02476396 Recruiting - Stroke Clinical Trials

Structural Stability of Carotid Plaque and Symptomatology

Start date: November 9, 2015
Phase:
Study type: Observational

The purpose of the research is to understand structural plaque abnormalities that make a carotid plaque unstable and brake off (embolize) which would help to predict and treat individuals who are likely to suffer not only classic episodic major strokes but also cognitive impairment.

NCT ID: NCT02476188 Completed - Acute Stroke Clinical Trials

Neutrophil Extracellular Traps and Thrombolysis in the Acute Stroke

NETs
Start date: July 31, 2015
Phase: N/A
Study type: Interventional

The purpose of the study was to investigate the correlation between the nucleosome concentration and the rate of recanalization after thrombolysis. All patients were admitted to the Stroke Unit at the University Hospital Sainte-Anne where they received standard stroke care. The investigators included all patients treated or not by intravenous thrombolysis for anterior circulation stroke with or without vessel occlusion. Exclusion criteria were neoplasms, chronic inflammatory diseases and cytostatic therapy at the time of stroke and stroke-specifics symptoms that had started earlier than 4.5 hours before admission.

NCT ID: NCT02475083 Completed - Stroke Clinical Trials

Use of Virtual Reality Games for the Treatment of Balance and Reducing the Occurrence of Falls in Patients After Stroke

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

The aim of this study was to investigate the therapeutic effect of virtual reality associated with conventional physiotherapy on balance during gait and the occurrence of falls in patients after stroke.

NCT ID: NCT02473549 Completed - Stroke Clinical Trials

Improving Motor Stroke Recovery Using Patient-tailored Non-invasive Brain Stimulation

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Many individuals are often left with problems moving their arm and hand, months to even years after a stroke. Recent progress in research suggests the application of non-invasive brain stimulation, such as transcranial direct current stimulation (TDCS), in conjunction with rehabilitation exercises can further improve a person's ability to move after stroke. However, the problem is that this doesn't work for everyone, and researchers do not know why. One reason may be that TDCS is currently applied using a one-size-fits-all approach. Researchers apply the same type of TDCS to everyone, assuming the stroke affects everyone in the same way. But, researchers know this is not the case. For example, each person will likely have different amounts of damage to brain regions that control movements. A better understanding of how the stroke uniquely affects a person's brain will help us to know which is the correct type of TDCS to apply for that person. Therefore, the objective of this research is to determine whether the amount of damage to brain regions that control movements can predict which type of TDCS will be more effective to help a person improve their ability to move. Participants will undergo 1 session of magnetic resonance imaging, and three sessions of TDCS.