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Cerebral Infarction clinical trials

View clinical trials related to Cerebral Infarction.

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NCT ID: NCT02777099 Recruiting - Ischemic Stroke Clinical Trials

Impact of Remote Ischemic Postconditioning on Autonomic Function in Stroke Patients

IRAS
Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether remote ischemic postconditioning (RIPostC) initiates autonomic nervous system response and affects the prognosis in patients with acute ischemic stroke.

NCT ID: NCT02776540 Completed - Clinical trials for Ischemic Cerebrovascular Accident

Clopidogrel for Acute Ischaemia of Recent Onset

CAIRO
Start date: June 1, 2016
Phase: Phase 4
Study type: Interventional

Evaluate the role of loading Clopidogrel in acute ischemic stroke in improving neurological outcome of stroke in cases patients will be non-eligible for, or declined, treatment with or intravenous thrombolysis with rTPA, rTPA is not available or thrombectomy.

NCT ID: NCT02767778 Terminated - Ischemic Stroke Clinical Trials

Low-frequency Pulsed Electromagnetic Fields (ELF-MF) as Treatment for Acute Ischemic Stroke

I-NIC
Start date: April 2016
Phase: N/A
Study type: Interventional

The main purpose of this multicentric, prospective, randomized, placebo-controlled, double-blind study is the validation of pulsed ELF-MF stimulation as non-invasive and safe tool to promote recovery in acute ischemic stroke patients. 124 patients with acute ischemic stroke will be recruited and randomly assigned to real or sham group. Patients will be stimulated with pulsed ELF-MF (75 Hz, 1,8 mT), for 120 min daily, for 5 consecutive days, starting within 48 hours from the onset of stroke. The primary outcome will consist of reduction of the expected infarct growth at MR measured in the subacute and chronic phase. Secondary outcomes will explore clinical effectiveness, safety and tolerability of pulsed ELF-MF in acute ischemic stroke.

NCT ID: NCT02752867 Recruiting - Clinical trials for Cognitive Impairment

An fMRI Study of Jianpi Yishen Huatan Granules for Cognitive Impairment After Acute Cerebral Infarction

Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the pathogenesis of cognitive impairment after acute cerebral infarction by applying the multimodal function MRI to dynamically observe the changes of the value of NAA,Cho,Cr,FA in a certain region in the brain and the function of the brain ,and to provide a visual instrument for evaluating the therapeutical effects of Chinese medicine through the application of multimodal function MRI to observe the changes of the neurotransmitter in certain area in the brain before and after the treatment.

NCT ID: NCT02730455 Completed - Clinical trials for Acute Ischemic Stroke

Safety and Efficacy of Intravenous Natalizumab in Acute Ischemic Stroke

ACTION2
Start date: July 18, 2016
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to assess the clinical effects of natalizumab versus placebo in acute ischemic stroke on clinical measures of functional independence and activities of daily living. The secondary objective of the study is to explore dose and exposure response and the clinical treatment effects of natalizumab versus placebo in acute ischemic stroke on the following: measures of independence, activities of daily living, neurologic function, quality of life, cognition, and safety and tolerability

NCT ID: NCT02728180 Active, not recruiting - Clinical trials for Acute Ischemic Stroke

Xingnaojing for Moderate-to-severe Acute Ischemic Stroke (XMAS)

XMAS
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The main purpose of this trial is to determine whether Xingnaojing, intravenously administered within 24 hours of symptom onset, improves the 3-month outcome in participants with acute ischemic stroke.

NCT ID: NCT02684825 Completed - Ischemic Stroke Clinical Trials

Detection of Silent Atrial Fibrillation aFter Ischemic StrOke

SAFFO
Start date: October 2015
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate whether, in patients with first-ever atherothrombotic or lacunar stroke without any previous history of atrial fibrillation (AF)/atrial flutter (AFL)/atrial tachycardia (AT), the detection of AF/AFL/AT (silent or symptomatic) by using a continuous cardiac rhythm monitoring with implantable loop recorder (ILR) during the first 12 months of observation is higher than the detection by using a standard cardiac monitoring (physical exam, 12-lead electrocardiogram [ECG] at baseline, 3, 6, and 12 months and Holter ECG at 3 months) in the same period of time.

NCT ID: NCT02678169 Completed - Ischemic Stroke Clinical Trials

European Registry on the ACE Reperfusion Catheters and the Penumbra System in the Treatment of Acute Ischemic Stroke

PROMISE
Start date: February 2016
Phase: N/A
Study type: Observational

Prospective, single-arm, multicenter, observational registry of the ACE Reperfusion Catheters and the Penumbra System in Europe. Consecutive patients presenting within 6 hours from symptom onset with an acute ischemic stroke (within the internal carotid artery and internal carotid terminus, middle cerebral - M1/M2 segments) due to anterior circulation large vessel occlusion (LVO) will be treated using the ADAPT technique with thrombo-aspiration as first intention and site routine practice.

NCT ID: NCT02643030 Completed - Cerebral Ischemia Clinical Trials

Hypercapnia During Shoulder Arthroscopy

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of hypercapnia on hemodynamics and cerebral oxygenation during shoulder arthroscopy.

NCT ID: NCT02641886 Completed - Clinical trials for Cognitive Impairment

The Study of Jian Pi Yi Shen Hua Tan Granules in Cognitive Impairment After Acute Cerebral Infarction

Start date: March 9, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the chinese medicine Jian Pi Yi Shen Hua Tan granules is effective in the treatment of cognitive impairment after acute cerebral infarction .