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Stroke clinical trials

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NCT ID: NCT02995265 Completed - Conditions Clinical Trials

Exoskeleton for Post-Stroke Recovery of Ambulation

ExStRA
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

To determine the effect of using a robotic exoskeleton to allow walking practice after stroke, compared to usual physiotherapy care, on recovery of walking ability and secondary outcomes.

NCT ID: NCT02995213 Completed - Stroke Clinical Trials

Quantification of UE Use and Effects of Feedback in the Home Setting

OPTASpr2016
Start date: November 2015
Phase: N/A
Study type: Interventional

The investigators are proposing a pilot study, the purpose of which is to use accelerometers to quantify UE use (1 and two hand use) in people post-stroke from which the investigators will develop use-based feedback to improve recovery in the home setting. The objectives of this pilot study are to: i.) determine the feasibility of using accelerometers to quantify amount of UE use in the home setting in individuals chronic post-stroke, ii.) quantify and compare the unilateral activity of the weaker (paretic) versus stronger (non-paretic) UEs, and iii.) assess the effect of a 7 sessions of in-home accelerometer used-based feedback on unilateral and bilateral UE use. iv.) assess kinematic, kinetic, and EMG data during UE movements unilaterally and bilaterally in subjects post-chronic stroke pre and post feedback.

NCT ID: NCT02993172 Completed - Stroke Clinical Trials

The Copenhagen City Heart Study

CCHS
Start date: January 1976
Phase: N/A
Study type: Observational

The Copenhagen City Heart Study is an ongoing cardiovascular population study initiated in 1976 which has examined approximately 25,000 individuals from the general population. The initial sample has been re-invited up to four times and supplemented by younger individuals. The study includes questionnaires, clinical assessment and biomarkers. The population have been followed in a number of outcome registries and more than 900 scientific papers have been published.

NCT ID: NCT02992821 Completed - Stroke Clinical Trials

Pocket Sized Carotid Stenosis Screening by Junior Doctors

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

Among patients admitted with cerebral ischemia (stroke and transitory ischemic attack (TIA)) it is important to reveal the underlying cause of the disease. In special it is important to reveal if carotid artery stenosis is present as such a finding will directly influence on treatment and follow-up. For the diagnosis of carotid artery stenosis due to atherosclerosis ultrasound examinations is the cornerstone, but computer tomography and magnetic resonance imaging may be better in some cases. Development of high quality pocket-sized ultrasound scanners has allowed for semi quantitatively bed-side assessment of the carotid arteries and the heart. The investigators aim to study the feasibility and reliability of bed-side assessment of the carotid arteries by pocket-sized ultrasound scanners in inexperienced hands and the clinical influence of this examination when performed by experienced users. The investigators hypothesize that a significant proportion of this patient population can be clarified bed-side by junior doctors with no need of further imaging procedures for the assessment of the carotid arteries and the heart.

NCT ID: NCT02990650 Completed - Clinical trials for Cerebrovascular Accident

Outcomes Associated With Progressive Balance And Gait Training Using The KineAssist® Robot

Start date: October 2008
Phase: Phase 1
Study type: Interventional

Using a randomized controlled research design, compare walking outcomes resulting from gait and balance training with standard physical therapist interaction versus training with the addition of a KineAssist® robotic system that provides for safety and freedom of movement.

NCT ID: NCT02989376 Completed - Stroke, Acute Clinical Trials

Carotid Duplex Ultrasound for Selecting Patients for Endovascular Thrombectomy in Acute Stroke Patients

ECHO-SELECT
Start date: October 2016
Phase: N/A
Study type: Interventional

The aim of this study is to address the usefulness of carotid duplex ultrasound as vascular imaging for selecting acute stroke patients for endovascular thrombectomy.

NCT ID: NCT02988492 Completed - Stroke Clinical Trials

Acute Stroke Thrombectomy: Does CT Perfusion Accurately Predict Infarct on MRI After Recanalization

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The newest generation of stent---retrievers results in higher recanalization rates and faster recanalization time compared to older generation endovascular therapies for acute stroke. Advanced neuroimaging can potentially improve the assessment of infarct core and inform decision---making in patients being considered for endovascular therapy. Evaluation of infarct core may be performed with NECT, CTASI or CT perfusion. In the past, evaluation of CTP in predicting core infarct in acute stroke has been limited because recanalization status was lacking. In addition, final infarct size may be underestimated on NECT compared with MRI. These two limitations can now be addressed: the new generation of stent---retrievers allows accurate determination recanalization time; evaluating the test characteristics of CTP using 24 hour DWI---MRI as the reference standard can be readily performed. We aim to prospectively investigate the sensitivity and specificity of whole---brain CTP in predicting 24 hour DWI---MRI infarct in patients with acute proximal anterior circulation occlusions successfully recanalized with endovascular treatment.

NCT ID: NCT02987361 Recruiting - Stroke Clinical Trials

Effect of tDCS on Upper Extremity After Strokes

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

The investigators hypothesize that transcranial direct current stimulation (tDCS) can improve upper limb motor recovery in the sub-acute phase of stroke patients. This is a randomized, controlled, double blind, cross-over, multicentre, clinical trial.

NCT ID: NCT02985463 Active, not recruiting - Stroke Clinical Trials

Left Atrial Appendage Occlusion and Biomarker Evaluation

LABEL
Start date: June 2014
Phase:
Study type: Observational

"Left Atrial Appendage Occlusion and Biomarker Evaluation" (LABEL) is a single-center, prospective and observational study evaluating changes of the expression of biomarkers in eligible patients before and after percutaneous implantation of a left atrial appendage (LAA) occlusion device at mid-term follow-up.

NCT ID: NCT02985060 Recruiting - Ischemic Stroke Clinical Trials

Mild Hypothermia After Endovascular Treatment in Acute Ischemic Stroke

HELMET
Start date: November 2016
Phase: Phase 2
Study type: Interventional

To study safety and feasibility of mild therapeutic hypothermia after successful recanalization by mechanical endovascular treatment in patients with acute ischemic stroke and proximal arterial occlusion.