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Stroke clinical trials

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NCT ID: NCT02982668 Terminated - Dysphagia Clinical Trials

Optimizing Early Enteral Nutrition in Severe Stroke

OPENS
Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this academic lead study is to explore the ideal nutritional support strategy for patient with acute severe stroke.

NCT ID: NCT02982655 Completed - Hypertension Clinical Trials

Controlling Hypertension After Severe Cerebrovascular Event

CHASE
Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this academic lead study is to explore ideal blood pressure targets and optimum individualized anti-hypertension strategies in acute severe stroke.

NCT ID: NCT02982278 Completed - Minority Health Clinical Trials

Wide Spectrum Investigation of Stroke Outcome Disparities on Multiple Levels (WISSDOM)

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

This research project will evaluate the relationship between cardiovascular risk factors, degrees of physical and mental activity prior to the stroke, brain tissue integrity, post-stroke community participation and neurological recovery after the stroke. Investigators will recruit and study healthy and post stroke participants, gaining insight into the possible mechanisms that explain why the adverse risk profile, which is more commonly present in African-Americans than non-Hispanic Whites in the stroke belt, is translated into a less favorable recovery post stroke.

NCT ID: NCT02980796 Recruiting - Stroke Clinical Trials

The Influence of Exercise on Neuroplasticity and Motor Learning After Stroke

EX-ML3
Start date: November 2016
Phase: N/A
Study type: Interventional

Participants will complete 11 sessions. These include screening, 5 sessions where exercise or rest (according to group assignment) are paired with practice of a motor task, MRI and Transcranial Magnetic Stimulation (TMS) before and after the intervention will be used to assess neuroplasticity (ability for the brain to reorganize and create new connections).

NCT ID: NCT02980744 Completed - Stroke Clinical Trials

A Home-based Intervention to Reduce Sedentary Behaviour and Improve Function After Stroke

STUFFS
Start date: August 2016
Phase: N/A
Study type: Interventional

The traditional approach to physical activity promotion in people with stroke has always emphasized activities of a moderate-to-vigorous intensity (i.e. moving enough to breathe fast and break a sweat). For many people with stroke who often have difficulty with walking, achieving that intensity of activity is difficult. The result is that people with stroke spend over 80% of their day in sedentary behaviours (too much sitting). A growing body of research shows that too much sitting has negative effects on health including larger waist circumference, unhealthy levels of blood glucose and insulin, heart disease, lower levels of functioning, and premature death. This project tests a new approach to activity promotion that focuses on increasing light-intensity activity throughout the whole day while reducing sitting time. The new intervention is titled "STand Up Frequently From Stroke (STUFFS)" and is aimed at increasing self-confidence among people with stroke to sit less, stand up and walk around at frequent intervals during the day. Studies in the general population have shown that standing up and walking around frequently are beneficially associated with health indicators (lower waist circumference, lower blood fat and glucose levels). Encouraging people with stroke to reduce sitting and increase light-intensity activities appears feasible and sustainable and might be a first step to increase their daily energy expenditure.

NCT ID: NCT02980354 Recruiting - Stroke Clinical Trials

Bayraktutan Dunhill Medical Trust EPC Study

Start date: February 1, 2017
Phase:
Study type: Observational

Stroke is a life-threatening medical condition that occurs due to a sudden disruption of blood supply to the brain. Although it may affect all age groups including children, the elderly are at a greater risk of having strokes. Indeed, three-quarter of all strokes are seen in people over the age of 65. Unfortunately, due to short therapeutic window (4.5 h of stroke onset), only 2-3% of patients can receive the currently available single medical therapy with rt-PA, a clot-busting agent. As recent studies show that bone marrow-derived endothelial progenitor cells, a type of stem cells, may migrate to the site of injury to repair the damaged brain vessels and tissue, it is possible that their numbers and functional capacity may determine the clinical outcome of stroke patients i.e. severely disabled, moderately disabled or no signs at all. This study will assess these parameters in elderly stroke patients compared to their age-matched stroke-free counterparts and healthy young volunteers.

NCT ID: NCT02979782 Completed - Delirium Clinical Trials

Neurological Outcome After Minimal Invasive Coronary Artery Bypass Graft

NOMICS
Start date: December 2016
Phase:
Study type: Observational

Primary objectives: Assessment of the incidence of postoperative cognitive dysfunction (POCD), cerebrovascular accident (CVA), and delirium after minimal invasive coronary artery bypass grafting (Endo-CABG). Secondary objectives: - Quality of life, three months after endo-CABG - Patient satisfaction with endo-CABG and the tests performed - The influence of various demographic and peri-operative variables on neurological outcome after endo-CABG - Incidence of fear and depression, 3 months after endo-CABG

NCT ID: NCT02978794 Active, not recruiting - Stroke Clinical Trials

Implementation of Clinical Pathway to Improve Quality of Healthcare in Stroke Inpatients

Start date: November 2016
Phase:
Study type: Observational

With the extension of the average life expectancy, the incidence of cardiovascular diseases is also rising. Stroke in Taiwan has been the leading cause of morbidity and mortality, but also in countries around the world), stroke and the impact of socio-economic and health spending are large how to reduce the degree of disability after stroke is an important issue in medicine. For a long time, the resident will fill the clinical pathway form before the stroke inpatients were discharged. We also analyzed the data of clinical pathway every three months. According to the current data of stroke clinical pathway included demographic data, length of hospitalization days, complications, functional independent measure, Brunnstrom motor recovery stage, mini-mental state examination, geriatric depression scale, blood pressure data, and post-stroke checklist for a retrospective analysis to provide more complete and more comprehensive information on follow-up care for stroke patients and effective use of medical resources, to improve the quality of future medical care and quality of life for stroke patients.

NCT ID: NCT02978079 Recruiting - Stroke Clinical Trials

Pupillometry in Horner's Syndrome

Start date: February 15, 2017
Phase: N/A
Study type: Interventional

Horner's syndrome (HS) is a result of interruption of the sympathetic innervation to the eye and ocular adnexa, which can occur due to carotid artery dissection (CAD), along which the sympathetic nerve fibers travel to reach the eye. Dissection of the carotid artery is one of the etiologies for ischemic stroke in young patients. In our current study, we will explore the diagnostic accuracy of automated binocular pupillometry in the diagnosis or HS, and its potential in identifying dissection of the carotid artery in patients of young age who suffer ischemic stroke.

NCT ID: NCT02977390 Completed - Fluid Therapy Clinical Trials

Passive Leg Raise Induced Stroke Volume Changes in Elderly Prior to Elective Surgery Measured by LiDCOplusTM

Start date: October 2013
Phase: N/A
Study type: Interventional

This is a pilot study to investigate whether patients at advanced age are fluid responders via a reversible fluid challenge, the passive leg raise test. This will be measured with a non-invasive cardiac output monitor, the LiDCO (LiDCO Hemodynamic monitoring) .