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Ischemic Stroke clinical trials

View clinical trials related to Ischemic Stroke.

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NCT ID: NCT04675762 Recruiting - Stroke Clinical Trials

Combinating Fingolimod With Alteplase Bridging With Thrombectomy in Acute Ischemic Stroke

Start date: January 15, 2021
Phase: Phase 2
Study type: Interventional

Proof-of concept clinical trials have indicated that the sphingosine-1-phosphate receptor modulator fingolimod may be efficacious in attenuating brain inflammation and improving clinical outcomes in patients with AIS as a single therapy beyond 4.5 hours of disease onset, or in combination with alteplase within 4.5 hours of disease onset. So in this study the investigators try to determine whether the addition of fingolimod, administered within 24 hours after the onset of symptoms in patients receiving alteplase bridging with mechanical thrombectomy, improves radiologic and clinical outcomes.

NCT ID: NCT04672148 Completed - Stroke, Ischemic Clinical Trials

Prognostic Factors and Mortality in Older Stroke Patients With Mechanical Thrombectomy

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

The study focus on the elderly patient (older than 80 years of age) who had acute ischemic stroke and received mechanical thrombectomy. The investigators analyze different factors in the stage of before, between, after procedure and trying to figure out if there is any difference between the 30-day-mortality group versus non-30-day-mortality group.

NCT ID: NCT04667637 Completed - Stroke Clinical Trials

Improving Neuroprotective Strategy for Ischemic Stroke With Sufficient Recanalization After Thrombectomy by Edaravone Dexborneol

Start date: February 23, 2021
Phase: Phase 2
Study type: Interventional

To explore the safety and efficacy of edaravone dexborneol for the treatment of acute ischemic stroke patients who received endovascular thrombectomy.

NCT ID: NCT04664946 Active, not recruiting - Ischemic Stroke Clinical Trials

Intra-arterial Neuroprotective Strategy for Ischemic STroke Patients With No Reperfusion Therapy (INSIST-NRT)

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

To explore the safety and feasibility of intra-arterial neuroprotective strategy in acute ischemic stroke patients who missed recanalization operation.

NCT ID: NCT04664933 Recruiting - Stroke, Ischemic Clinical Trials

Intra-arterial Neuroprotective Strategy for Ischemic STroke Patients With Endovascular Therapy (INSIST-ET)

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

To explore the safety and feasibility of intra-arterial neuroprotective strategy in acute ischemic stroke patients who received recanalization operation.

NCT ID: NCT04663399 Recruiting - Ischemic Stroke Clinical Trials

IMMunological resPonse Assessment afteR Acute iSchemic Stroke Treated With Endovascular Therapy (IMPRESS)

IMPRESS
Start date: February 23, 2023
Phase:
Study type: Observational

IMPRESS study aims to describe the immuno-inflammatory and thrombo-inflammatory profiles during the first 24/36 hours of treatment of patients suffering from AIC treated with TM, and to study the possible impact of these profiles on the functional prognosis at 3 months of AIC treatment.

NCT ID: NCT04651010 Recruiting - Clinical trials for Middle Cerebral Artery Acute Ischemic Stroke

Predictive Multimodal MRI Factors in Subacute Cerebral Artery Occlusiontreated by Thrombectomy (PIMISUTT)

PIMISUTT
Start date: November 15, 2021
Phase: N/A
Study type: Interventional

Our study aims to measure metabolic and functional parameters of the infarcted territory by multimodal cerebral MRI in patients diagnosed with unilateral proximal occlusion of the middle cerebral artery and treated by thrombectomy in order to correlate those parameters to clinical outcome (evaluated by modified Rankin score) at 3 months. We aim to find early radiologic predictive factors for favorable clinical outcome in this population of patients.

NCT ID: NCT04650022 Completed - Ischemic Stroke Clinical Trials

Total Posterior-circulation Infarct Volume in Basilar Artery Stroke

TPCIV-ABAO
Start date: January 30, 2011
Phase:
Study type: Observational

Preprocedural predictors of outcome in patients with acute basilar artery occlusion (ABAO) who underwent endovascular treatment (EVT) remain controversial. The Investigators aimed to analyse, in patients with ABAO treated by EVT, if pre-EVT DWI total posterior-circulation infarct volume (TPIV) was a predictor of 90-days outcomes

NCT ID: NCT04647292 Recruiting - Ischemic Stroke Clinical Trials

European Blood Pressure Intensive Control After Stroke

EPICS-Pilot
Start date: May 2, 2024
Phase: Phase 2
Study type: Interventional

Stroke is the third most common cause of death worldwide and the leading cause of disability. High blood pressure is an important risk factor for stroke. Lowering a person's blood pressure reduces the risk of future stroke or heart attack, and current guidelines recommend treatment to a target of <130mmHg for secondary prevention. Home blood pressure measurement and telemonitoring are acceptable to patients, but there is uncertainty over the use of out of office blood pressure measurements in stroke patients in guidelines. This is a study designed to establish the feasibility of a larger clinical trial, comparing home blood pressure monitoring, telemonitoring and medication titration with standard care. The study hypothesis is that home BP measurement and telemonitoring with medication titration may lead to improved BP control compared to standard of care clinical practice.

NCT ID: NCT04644679 Terminated - Stroke Clinical Trials

Monitoring Strategies for the Detection of Atrial Fibrillation in Patients With Cryptogenic Stroke

Start date: November 2, 2020
Phase: N/A
Study type: Interventional

Randomized clinical trial comparing two monitoring strategies, the use of a 48-hour Holter (routine care branch) and an event recorder for 7 days (intervention branch). Patients admitted for cryptogenic stroke will be included. Enrollment and randomization of patients will be carried out during the index case hospitalization, while follow-up will be done on an outpatient basis until day 7.