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Stroke, Ischemic clinical trials

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NCT ID: NCT04622644 Recruiting - Stroke, Ischemic Clinical Trials

Clinical Investigation to Evaluate the Suitability of StrokeWave in Distinguishing Haemorragic From Ischaemic Strokes

Start date: February 23, 2021
Phase: N/A
Study type: Interventional

This is a pilot, monocentric clinical investigation to evaluate the suitability of StrokeWave in distinguishing haemorragic from ischaemic strokes. The StrokeWave is a microwave device which employs a novel technique to generate images by processing very low power (<1mW) microwaves. The trial design has been developed in order not to interfere with thw standard diagnostic approach used for the hyperacute stroke patients, nor to modify the usual standard timing of the routine assessment.

NCT ID: NCT04608617 Recruiting - Stroke, Ischemic Clinical Trials

SYNCHRONISE: LVO Triage Timing and Outcome Study

Start date: March 9, 2021
Phase:
Study type: Observational

The objective of this study is to evaluate the impact of Viz LVO in hospital systems with non-interventional and interventional (spoke and hub) stroke centers on the timing and outcomes of patients with suspected acute ischemic stroke indicated for mechanical thrombectomy.

NCT ID: NCT04607070 Recruiting - Atherosclerosis Clinical Trials

Ischemic Strokes While on NOAC - How Compliance Matters

Start date: October 1, 2020
Phase:
Study type: Observational

This study is aimed to depict the epidemiological trend, aetiologies, clinical characteristics, treatment options of IS-NOAC in face of the rapidly increasing NOAC usage. Knowledge on this ischaemic stroke entity will define clinical characteristics, identify preventable causes and inform resource allocation on the evaluation modalities, reperfusion strategies and forecast future burden of IS-NOAC.

NCT ID: NCT04555538 Recruiting - Atrial Fibrillation Clinical Trials

Atrial CMR in Patients With CVA of Unknown Source and no Known AF

CARM-AF
Start date: October 1, 2020
Phase:
Study type: Observational

This research study will investigate a new method for identifying which patients should be offered blood thinners or therapies to reverse the underlying causes after stroke. Atrial fibrillation(AF) is the primary risk factor for ischaemic stroke, increasing the risk by up to 5-fold. In AF, the upper heart chambers don't pump blood effectively into the lower chambers. When this happens, a blood clot can form, dislodge and leave the heart blocking an artery in the brain and cause a stroke. However, AF is often an intermittent condition and therefore difficult to diagnose. As such, there are a group of patients in whom no cause of their stroke can be identified. In this study, we will recruit 92 patients from Guy's and St Thomas' Hospital, Princess Royal University Hospital and King's College London. As part of routine clinical care, patients undergo insertion of an Implantable Loop Recorder (CE Marked device), a minimally invasive procedure that allows accurate beat-to-beat monitoring to identify patients who develop intermittent AF post-stroke. We will request access to the data collected from this device and perform atrial MRI imaging in these patients to compare the findings between patients that do and do not have AF. If we show that atrial MRI scans are significantly different between patients with and without AF, we will use this information to support a trial of starting appropriate therapies (e.g. blood thinners) in these patients on the basis of MRI findings. This approach would have the advantage of enabling therapies to be offered to the right patients earlier and prevent repeat, potentially disabling stroke.

NCT ID: NCT04412434 Recruiting - Stroke, Ischemic Clinical Trials

EEG Patterns in Patients With Acute Ischemic Stroke Resulted From Large Vessels Occlusion in the Anterior Circulation

Start date: October 4, 2020
Phase: N/A
Study type: Interventional

Clinical deterioration is observing in up to forty percent of patients with acute ischemic stroke (AIS) due to large vessels occlusion. Until now, there is no automated monitoring system for early detection of neurological deterioration in such patients. As a first step to develop such system investigators suggest this study aiming to evaluate patterns of brain electrical activity registered by EEG in patients with AIS attributed to the MCA or ICA territory correlated with location and extension of ischemic lesions as determined by non-contrast CT (NCT).

NCT ID: NCT04408261 Recruiting - Clinical trials for Coronary Artery Disease

BuqitongluO Granule for Qi Deficiency and Blood Stasis Syndrome

BOSS
Start date: July 22, 2020
Phase: Phase 2
Study type: Interventional

The main purpose of this trial is to evaluate the efficacy and safety of Buqitongluo Granule in treating qi deficiency and blood stasis syndrome, and explore the effect of the improvement of qi deficiency and blood stasis syndrome on the prognosis of diseases.

NCT ID: NCT04321512 Recruiting - Clinical trials for Myocardial Infarction

Study of Circulating Monocytes in Patients With Ischemic Vascular Disease

Start date: December 1, 2013
Phase:
Study type: Observational

The purpose of this research study is to discover the functions of circulating white blood cells, called monocytes, and associated circulating substances in heart attack and ischemic stroke patients. Ischemic Strokes (clots) occur as a result of an obstruction within a blood vessel supplying blood to the brain. A type of monocyte carrying a surface marker called "P2X4" helps the immune system sense and respond to danger signals from the body such as heart muscle and brain tissue injuries. The researchers expect to learn more about how these monocyte cells react to heart and brain tissue injury, and how the cells may then produce proteins or other chemical substances which promote the healing of heart muscle after heart attack and brain tissue after an ischemic stroke.

NCT ID: NCT04282993 Recruiting - Atrial Fibrillation Clinical Trials

Wearable Devices for Secondary Prevention of Ischemic Stroke

Start date: April 16, 2019
Phase: N/A
Study type: Interventional

Ischemic stroke is an important cause of death and disability in Western countries. Different risk factors have been identified such as hypertension, diabetes, dyslipidemia, smoke, atrial fibrillation, obesity, and sedentary. The aim of this study is to evaluate the feasibility of an approach based on the use of wearable devices for the identification and reduction of risk factors in patients with previous history of ischemic stroke or transient ischemic attack.

NCT ID: NCT04256096 Recruiting - Stroke, Ischemic Clinical Trials

Randomization of Endovascular Treatment in Acute Ischemic Stroke in the Extended Time Window

RESILIENTExt
Start date: March 9, 2020
Phase: Phase 3
Study type: Interventional

A phase III, randomized, multi-center, open label clinical trial that will examine whether endovascular treatment is superior to standard medical therapy alone in patients who suffer a large vessel anterior circulation ischemic stroke within 8-24 hours from time last seen well

NCT ID: NCT04230785 Recruiting - Stroke, Acute Clinical Trials

Circulating Non-coding RNA in Acute Ischemic Stroke With Endovascular Treatment (EVTRNA)

EVTRNA
Start date: March 15, 2020
Phase:
Study type: Observational [Patient Registry]

EVTRNA is to analyze the differentiated expression pattern of circular RNA (circRNA), long non-coding RNA (lncRNA) and micro-RNA (miRNA) by next-generation sequencing in acute ischemic stroke patients before and/or after endovascular treatment. The candidate circRNA/lncRNA/miRNA will be verified as the biomarker and regulator for progression and prognosis of acute ischemic stroke with endovascular treatment. Further, the candidate non-coding RNA will be used to evaluate the effect of endovascular treatment on both peripheral and central immune after stroke.