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Stroke clinical trials

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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: NCT02702375 Active, not recruiting - Stroke Clinical Trials

Meta-analyses of Impotrant Food Sources of Sugars and Incident Cardiometabolic Diseases

Start date: September 2015
Phase: N/A
Study type: Observational

There is an urgent need for stronger evidence to support recommendations for the role of sugars in diabetes and related cardiometabolic diseases. Although large prospective cohort studies have shown a significant positive association of fructose-containing sugars-sweetened beverages with incident obesity, diabetes, heart disease, and stroke, these associations do not appear to hold true for total fructose-containing sugars and other important sources of free fructose-containing sugars such as pure fruit juice, yogurt, or even cakes and sweets. As dietary guidelines have moved away from macronutrient centric recommendations towards more food and dietary-pattern based recommendations, this inconsistency in the data has not been appreciated. There remains a focus on free sugars, in the absence of sufficient information on the role of different food sources of fructose-containing sugars in diabetes and related cardiometabolic diseases. A systematic review and meta-analysis of prospective cohort studies is considered to be the "Gold Standard" of evidence. To provide evidence-based guidance to support the development of public health policy in relation sugars and the primary prevention of diabetes, we will conduct a series of systematic reviews and meta-analyses of the relation of food sources of fructose-containing sugars with incident type 2 diabetes and related cardiometabolic diseases in prospective cohort studies.

NCT ID: NCT02700061 Active, not recruiting - Stroke Clinical Trials

Effects of Upper Limb Motor and Robotic Training Over Neuroplasticity and Function Capacity

NARLE1
Start date: February 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate and compare the effects of upper limb training with Induced Constraint Therapy (ICT) or robotic therapy. No placebo therapy is used. Motor function, neurological evaluations and quality of life are assessed for the comparison of the therapies.

NCT ID: NCT02673931 Active, not recruiting - Stroke Clinical Trials

GLP-1 and Hyperoxia for Organ Protection in Heart Surgery

GLORIOUS
Start date: February 2016
Phase: N/A
Study type: Interventional

Patients undergoing open heart surgery are at risk of suffering damage to the heart, brain and kidneys. This study is designed as a 2-by-2 randomized clinical trial with the purpose of investigating the organ protective effects of the glucagon-like-peptide-1 (GLP-1) agonist Exenatide versus placebo and restrictive versus liberal oxygenation during weaning from cardio-pulmonary bypass.

NCT ID: NCT02635685 Active, not recruiting - Stroke Clinical Trials

Clinical Decision Support for Stroke Prevention in Atrial Fibrillation

CDS-AF
Start date: January 11, 2016
Phase: N/A
Study type: Interventional

A cluster randomised study in the primary care setting to evaluate a electronic clinical decision tool for stroke prophylaxis in patients with atrial fibrillation.

NCT ID: NCT02582502 Active, not recruiting - Stroke Clinical Trials

Hyperbaric Oxygen Post Established Stroke

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

The purpose of this study is to examine the role of Hyperbaric Oxygen Therapy (HBOT) in improving neurological function in patients who are 6 to 36 months post ischemic stroke.

NCT ID: NCT02563886 Active, not recruiting - Clinical trials for Cerebrovascular Accident

Electrically Assisted Movement Therapy

EAMT
Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether intensive, focused training of the affected upper extremity after stroke results in long-term functional gains in moderately-to-severely paralyzed patients, more than 6 months after their vascular accident. During the course of therapy, user's attempts to move and complete exercises are assisted by neuromuscular electrical stimulation.

NCT ID: NCT02554487 Active, not recruiting - Stroke Clinical Trials

Early Sleep Apnea Treatment in Stroke

eSATIS
Start date: August 13, 2015
Phase: N/A
Study type: Interventional

Investigating the interrelation of stroke and sleep-disordered breathing (SDB) is of major importance. First because of the high occurrence rate of stroke and the fact that it is a frequent cause of long-term disability in adulthood. Second because SDB (obstructive, central and mixed forms) affects more than 50% of stroke survivors and has a detrimental effect on clinical stroke outcome. Third, spontaneous and learning-dependent sleep-associated neuroplasticity may be affected by SDB following stroke worsening stroke rehabilitation. Therefore, it is crucial to investigate whether early treatment of SDB with Adaptive Servo-Ventilation (ASV), the treatment device of choice to treat obstructive, central and mixed forms of SDB, has a beneficial effect on the evolution of the lesion volume and on clinical stroke outcome. To this end, the investigators recruit and prospectively follow 3 groups of patients with ischemic stroke over 1 year. During the first night after hospital admission due to acute stroke, nocturnal breathing is assessed by means of a respiratory polygraphy. Patients with significant sleep disordered breathing, defined as an Apnea-Hypopnea-Index (AHI) > 20/h, are randomized to ASV treatment or no treatment (sSDB ASV+ or sSDB ASV-). ASV treatment starts the second night following hospital admission and ends 90 days later. Stroke patients without SDB (AHI < 5 / h) serve as a control group (no SDB) to observe the evolution of the lesion volume and stroke outcome without the additional burden of SDB. Lesion volume one day after hospital admission due to acute stroke (after potential lysis therapy) measured by Diffusion Weighted Imaging will be subtracted from lesion volume measured by T2-weighted volumetry assessed 90(+/-7) days following stroke and compared between patients with and without ASV treatment (sSDB ASV+ and sSDB ASV-) as well as patients without SDB (no SDB). Short- and long-term clinical stroke outcomes are assessed by clinical scales and questionnaires 4 to 7 days, 3 months and 1 year following stroke. Cognitive outcome is assessed during hospitalization (within the first week following stroke) and after the treatment period of 90 days by neuropsychological tests assessing attention and memory. In addition, baseline assessment of physiological parameters such as blood pressure and endothelial function/arterial stiffness are assessed during the first weeks following stroke and at the end of the treatment period, i.e. approximately 90 days following stroke.

NCT ID: NCT02540096 Active, not recruiting - Stroke Clinical Trials

Effects of Mental Practice for Mobility in Post-stroke Hemiparesis

Start date: November 2015
Phase: N/A
Study type: Interventional

Stroke is a neurovascular event characterized by impaired blood supply to the brain due to rupture or obstruction of certain cerebral arteries, which often results in hemiparesis and can affect individuals of any age and sex, being prevalent in the elderly population. Among the main treatments available for stroke rehabilitation, most of them demands an appropriate structure and high-qualified personnel. Searching for more affordable treatment options, several studies suggest the use of mental practice with motor imagery as a potential therapeutic tool, since it can be performed at any place or any time the patient wishes, including their own homes. Motor imagery can be defined as the covert cognitive process of imagining a movement of your own body(-part) without actually moving that body(-part). Within this context, the objective of this study is to investigate the effects of mental practice for mobility, gait function and speed and muscle strength of the lower limb in subacute post-stroke hemiparesis.

NCT ID: NCT02504073 Active, not recruiting - Stroke Clinical Trials

Clinical Reasoning Process of Physiotherapists When Observing Hemiplegic Gait

Start date: March 2015
Phase: N/A
Study type: Observational

The goal of this study is to find out what clinical reasoning process physiotherapists undergo when observing hemiplegic patients gait.