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Stroke clinical trials

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NCT ID: NCT01738412 Not yet recruiting - Stroke Clinical Trials

Validation of an Electroencephalograph Based Algorithm for Detection of Onset and Deterioration of Acute Ischemic Stroke by Comparison to NIHSS

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is the validation of an Electroencephalograph based algorithm for detection of onset and deterioration of Acute Ischemic Stroke by Comparison to NIHSS.

NCT ID: NCT01737749 Not yet recruiting - Stroke Clinical Trials

Validation of Neurokeeper's Algorithm on Patients Undergoing Cardiac Surgery.

Start date: n/a
Phase: N/A
Study type: Observational

The primary objective of the study is to check the ability of Neurokeeper's algorithm system to detect and monitor changes in cerebral electrophysiological parameters as compared to clinical evaluation in patients undergoing cardiac surgery. The secondary objectives is correlations of EEG + ERP measurements with clinical evaluations as assessed by NIHSS ThiS study is a prospective, open label, single arm, self control, single center study. This study will be conducted in 50 subjects according to the inclusions/exclusions criteria.

NCT ID: NCT01723046 Not yet recruiting - Stroke Clinical Trials

Therapeutic Effects of a New Upper Limb Robot Assisted Therapy Device for Persons After Stroke

ARTHE
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to investigate the clinical effects of a new upper limb robot assisted therapy device that is linked to a virtual therapy environment in patients with stroke.

NCT ID: NCT01672515 Not yet recruiting - Stroke Clinical Trials

Protective Effects of Remote Limb Ischemic Preconditioning on Acute Cerebral Infarction

Start date: October 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Stroke is one of the three leading causes of human death, and a major cause of adult disability. Our pre-clinical studies confirmed that ischemic preconditioning can prevent cerebral infarction. Animal studies confirmed that ischemic postconditioning can reduce infarct size of cerebral infarction. Investigators hypothesized that postconditioning would reduce infarct volume of ischemic stroke patients.

NCT ID: NCT01632410 Not yet recruiting - Stroke Clinical Trials

The Autonomic Nervous System State and Response to Different Stimuli Among Patients Post Stroke: A Follow-up Study

Start date: July 2012
Phase: N/A
Study type: Observational

The study describes the autonomic control system function in subjects post stroke in comparison with healthy subjects. Aims: To describe the Autonomic hart rate control system function in post stroke subjects in different rehabilitation levels in comparison with healthy subjects. To examine the reflective reaction of the autonomic control system as reflected in the heart rate variability to stimulations subjects in different rehabilitation levels in comparison with healthy subjects. To examine the autonomic control system reaction as reflected in the heart rate variability to physical and cognitive action subjects in different rehabilitation levels in comparison with healthy subjects.

NCT ID: NCT01487746 Not yet recruiting - Ischemic Stroke Clinical Trials

Presence of Minor Anti Phospholipid Antibodies in Blood Samples of Ischemic Stroke Patients and Healthy Controls

Start date: December 2011
Phase: N/A
Study type: Observational

The investigators expect to find higher levels of both classical and minor antiphospholipid (APL) antibodies among the stroke cases. Furthermore, the investigators expect to find not only classical APLA but also minor antibodies. The investigators believe that minor antibodies have a major role in the hypercoagulability state.

NCT ID: NCT01473277 Not yet recruiting - Stroke Clinical Trials

Botulinum Toxin Type A (BT-A) in Hemiplegic Shoulder Pain Versus Steroid

Start date: January 2012
Phase: Phase 2
Study type: Interventional

The aim of this study is to confirm the efficacy and safety of the intra-articular injection of BT-A in a multicentric double blind randomised study. For this purpose intra-articular injection of BT-A will be compared with the intra-articular steroid injection that is the current "gold standard" for the treatment of HSP.

NCT ID: NCT01469858 Not yet recruiting - Stroke Clinical Trials

Perception and Multisensory Integration in Neurological Patients Using fMRI

Start date: November 2011
Phase: N/A
Study type: Interventional

The main objective of the study is to explore and map brain areas involved in sensory perception and multisensory integration in patients with central or peripheral neurological damage. The investigators hypothesize for example, that a change (compare to healthy subjects) in the perceptual maps and body representation could be detected and characterize in patients suffering from impairments of peripheral nerve conduction.

NCT ID: NCT01438593 Not yet recruiting - Ischemic Stroke Clinical Trials

Study of Purified Umbilical Cord Blood CD34+ Stem Cell on Chronic Ischemic Stroke

Start date: January 2013
Phase: Phase 1
Study type: Interventional

The purpose of the study is to determine the safety and possible effectiveness of brain transplants of CD34+ stem cells obtained from umbilical cord blood (UCB) to treat stroke.

NCT ID: NCT01376609 Not yet recruiting - Ischemic Stroke Clinical Trials

The Correlation Between Outcome and Infarct Growth in Patients With Acute Ischemic Stroke

COIG
Start date: August 2011
Phase: N/A
Study type: Observational

Previous research has shown there wasn't inevitable relationship between mismatch area and infarct growth according to Volumetric-subtraction mismatch volume.The recently published on Stroke paper has proposed Coregistration mismatch to calculate the mismatch to replace ischaemic penumbra, and it reignites hope for clinical application of the PWI/DWI mismatch. But the correlation between the mismatch, calculated by Coregistration mismatch method,and the clinical outcome of the patients with acute ischemic stroke is still unknown. so the investigators plan to conduct a prospective observational cohort study.