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Cerebral Infarction clinical trials

View clinical trials related to Cerebral Infarction.

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NCT ID: NCT04479449 Completed - Ischemic Stroke Clinical Trials

Efficacy and Safety of SP-8203 in Patients With Ischemic Stroke Requiring rtPA

SP-8203-2002
Start date: March 18, 2019
Phase: Phase 2
Study type: Interventional

This clinical trial is designed to evaluate the efficacy and safety of the combination therapy of SP-8203 (Otaplimastat) and recombinant tissue Plasminogen Activator (rtPA) standard of care. In this clinical trial, rtPA will be injected intravenously using an infusion device. If reperfusion is not occur in spite of rtPA therapy, endovascular therapy can be performed.

NCT ID: NCT04475328 Completed - Clinical trials for Acute Ischemic Stroke

Efficacy and Safety of AngongNiuhuang Pill in Patients With Acute Ischemic Stroke (ANGONG TRIAL)

Start date: October 1, 2020
Phase: Phase 3
Study type: Interventional

AngongNiuhuang pill has obvious effects on the cardiovascular and cerebrovascular diseases. Pharmacological experiments confirmed that AngongNiuhuang pill can protect blood-brain barrier, inhibit capillary permeability, improve the tolerance of cerebral ischemia and hypoxia, reduce oxidative stress injury, thus protecting brain tissue. Clinical studies have also confirmed that AngongNiuhuang pill can increase the GCS score, reduce coma, improve nerve function defect and promote nerve function recovery. The primary purpose of this trial was to evaluate the difference in the volume of cerebral infarction and cerebral edema between Angong Niuhuang pill and placebo in patients with ischemic stroke at 14 days compared with the baseline.

NCT ID: NCT04463563 Completed - Cardiac Surgery Clinical Trials

Cerebral Oximetry in Cardiac Surgery to Reduce Neurological Impairment and Hospital Length-of-stay

Start date: February 1, 2011
Phase: N/A
Study type: Interventional

Cerebral oximetry using near-infrared spectroscopy (NIRS) has been shown to reduce the incidence of neurological dysfunction and hospital length-of-stay in adult cardiac surgery though not all studies agree. A previous audit using cerebral saturations at or above baseline showed improved neurological and length-of-stay outcomes.

NCT ID: NCT04453800 Completed - Clinical trials for Acute Ischemic Stroke

The Efficacy and Safety of Sofadil for Injection in the Treatment of Acute Ischemic Stroke

Start date: October 1, 2016
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of sofadil injection in the treatment of acute ischemic stroke

NCT ID: NCT04449523 Recruiting - Silent Stroke Clinical Trials

Incidence of Silent Atrial Fibrillation in Patients With Clinically Silent Brain Ischemic Lesions

SILENT2
Start date: September 8, 2020
Phase:
Study type: Observational

Arterial Fibrillation (AF) is well-recognized as a cause for cryptogenic Acute Ischemic Stroke (AIS) and is associated with Silent Brain Infarction (SBI). However, the role of AF in the formation of lesions (SBIs) is less well established than its role in AIS and needs clarification. The investigators hypothesize that continuous rhythm monitoring will yield a similar incidence of AF diagnosis in patients with SBI as compared to patients with cryptogenic AIS. The primary objective is to assess the cumulative incidence of AF diagnosis at 24 months in patients with SBI.

NCT ID: NCT04437862 Completed - Acute Stroke Clinical Trials

A Study to Evaluate the Q Revascularization System for Neurointervention in Acute Ischemic Stroke

EvaQ
Start date: October 27, 2020
Phase: N/A
Study type: Interventional

Assess the safety and efficacy of the Q Revascularization System to remove thrombi and emboli from the neurovasculature in patients experiencing an acute ischemic stroke

NCT ID: NCT04431609 Recruiting - Carotid Arteries Clinical Trials

Carotid Web Associated With Cerebral Infarctions

CAROWEB
Start date: June 19, 2019
Phase:
Study type: Observational [Patient Registry]

Carotid Web located at the bulb level is a rare condition and is often associated with severe cerebral infarction in the carotid territory. This condition has been described predominantly in the black population. However, limited data are available for the epidemiology of carotid web and often result from selected population studies. It has been shown that the carotid web is a focal intimal dysplasia. Rate of ischemic stroke recurrence is high, even in patients treated with antiplatelet therapy. This subtle lesion is often unknown and misdiagnosed including in stroke unit. We assume that the implementation of a multicentric cohort would allow a comprehensive analysis of the carotid web condition.

NCT ID: NCT04425590 Recruiting - Ischemic Stroke Clinical Trials

The Benefit of Add On DLBS1033 for Ischemic Stroke Patient

Start date: April 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Stroke is one of the most common non-communicable diseases worldwide. It is the leading cause of morbidity and mortality in many countries. Stroke is broadly classified into ischemic and hemorrhagic stroke. Ischemic stroke is more common than hemorrhagic stroke. In Indonesia, the prevalence of ischemic stroke is 42.9% compare to hemorrhagic stroke 19.9%. Ischemic stroke defined as an episode of neurological dysfunction caused by focal cerebral, spinal, or retinal infarction. One of the main therapy in ischemic stroke is administration of anti thrombotic agent. DLBS1033 is a bioactive protein fraction isolated from Lumbricus rubellus. DLBS1033 possessed quadruple activities that inhibit platelet aggregation, induces fibrinogenolysis, fibrinolysis, and thrombolysis. This is a new proposed medication nowadays. There is still a limited study about DLBS1033. To our knowledge, research concern on the usage of DLBS1033 in stroke patients is very limited in Indonesia. This study aimed to Measure the benefit of DLBS1033 as add on therapy for ischemic stroke patients. The hypothesis of this study : a. The use of DLBS1033 improve functional status of ischemic stroke patients at hospital discharge. b. The use of DLBS1033 improve functional status 30-days after stroke onset.

NCT ID: NCT04415164 Recruiting - Clinical trials for Acute Ischemic Stroke

Evaluation of Xueshuantong in Patients With AcutE IschemiC STroke

EXPECT
Start date: September 29, 2020
Phase: Phase 4
Study type: Interventional

The aim is to assess the effects and harms of Xueshuantong lyophilized powder versus placebo in patients with acute ischemic stroke when initiated within 72 hours of symptom onset.

NCT ID: NCT04412850 Not yet recruiting - Stroke Clinical Trials

Intravenous Magnesium Sulphate in Acute Ischemic Stroke

Start date: December 1, 2020
Phase: Early Phase 1
Study type: Interventional

Magnesium has a neuroprotective role so the investigators aim to evaluate the role of intravenous magnesium sulphate in improving the clinical outcomes as assessed by the NIH Stroke Scale (NIHSS) in patients with acute ischemic stroke.