Clinical Trials Logo

Stroke clinical trials

View clinical trials related to Stroke.

Filter by:

NCT ID: NCT00608582 Completed - Aphasia Clinical Trials

Transcranial Magnetic Stimulation to Improve Speech in Aphasia

Start date: July 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine whether repetitive transcranial magnetic stimulation (rTMS) can be used to improve speech in chronic stroke patients with aphasia. Aphasia patients can have problems with speech production. The rTMS procedure allows painless, noninvasive stimulation of human cortex from outside the head. Chronic aphasia patients have been observed in our functional magnetic resonance brain imaging studies to have excess brain activation in brain areas possibly related to language on the right side of the brain (opposite side to where the stroke took place). It is expected that suppression of activity in the directly targeted brain region will have an overall modulating effect on the neural network for naming (and propositional speech) and will result in behavioral improvement.

NCT ID: NCT00604877 Active, not recruiting - Stroke Clinical Trials

Effects of Exercise on Endothelial Function in Stroke Patients

Start date: August 2003
Phase: N/A
Study type: Interventional

This study examines the hypothesis that 6 months of treadmill aerobic exercise training improves fibrinolysis (clot defense mechanism) and vasomotor function in chronic hemiparetic (muscular weakness or partial paralysis restricted to one side of the body) stroke patients compared to a control intervention, and that these changes are associated with reduced plasma insulin levels and improved insulin sensitivity / glucose metabolism in this population.

NCT ID: NCT00604747 Completed - Stroke Clinical Trials

Practice Structure on Motor Learning in Post-Stroke Patients

Start date: August 2006
Phase: N/A
Study type: Interventional

Background: The literature indicates that, in relation to motor learning, healthy subjects benefit more from random practice than from constant practice. However, this effect is not well known in post-stroke patients. Objective: The goal of this study was to investigate the effects of practice structure on motor learning in post-stroke patients. Methods: Participants included an experimental group (EG) of post-stroke patients: 17 males and females; and a control group (CG) of healthy individuals: 17 males and females. At the acquisition phase, all participants performed 30 trials of a coincident timing task. Nine individuals from each group practiced constantly (C) at a stimulus propagation speed of 3 mph, and eight from each group practiced randomly (R) at speeds of 2, 3, and 5 mph. Subsequent phases included: 1) transfer, 2) retention after 15 minutes, and 3) retention after 3 days. Each of these phases included 20 trials: 10 at a speed of 1 mph, and 10 at a speed of 4 mph. Intra- and inter-group comparisons were made employing an alpha level of 0.05 (5%).

NCT ID: NCT00604630 Completed - Stroke, Acute Clinical Trials

Multicenter Efficacy Study of Recombinant Human Erythropoietin in Acute Ischemic Stroke

ESS
Start date: January 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this randomized, double-blind, placebo-controlled multicenter study is to determine in a cohort of 506 patients with acute ischemic stroke in the middle cerebral artery territory, the effect of a three-day high-dose, intravenous erythropoietin treatment on functional outcome up to a follow-up of 90 days.

NCT ID: NCT00600379 Completed - Stroke Clinical Trials

Virtual Reality Training Program for Ambulatory Patients With Chronic Gait Deficits After Stroke

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the feasibility and efficacy of a virtual reality program for ambulatory patients with mild-to-moderate chronic gait deficits after stroke.

NCT ID: NCT00600327 Completed - Clinical trials for Transient Ischemic Attack

Carotid Artery Revascularization Using the Boston Scientific EPI Filter Wire EZ™ and the EndoTex™ NexStent™

CABERNET
Start date: December 2001
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to demonstrate the safety of the NexStent for treatment of carotid artery lesions undergoing stenting with adjunctive use of the FilterWire distal embolic protection device. The rates will be compared to an Objective Performance Criterion (OPC) derived from historic data from high-risk patients undergoing surgical intervention with Carotid endarterectomy. Patients included in this study are those at higher risk for complications associated with CEA.

NCT ID: NCT00600184 Terminated - Stroke Clinical Trials

Clinic-Based AMES Treatment of Stroke

AMES
Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The AMES device a investigational device which cyclically rotates the ankle while muscle vibrators stimulate sensory receptors in the muscles opposite to the joint being rotated. In effect, the device provides assisted movement of a joint and enhanced sensation of that movement. The purpose of this study is to determine whether stroke survivors who remain unable to move normally more than one year after their stroke will be able to walk and move their affected leg significantly better after treatment with a new robotic therapy, the AMES device.

NCT ID: NCT00597974 Completed - Stroke Clinical Trials

Neurological Outcome With Carotid Artery Stenting

CAS
Start date: September 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine how well patients undergoing carotid artery angioplasty and/or stent-supported angioplasty for the treatment of carotid artery stenosis will perform on a battery of tests to assess brain function before and after the procedure. This study will serve as a pilot project: (a) to determine incidence of neurologic/neuropsychometric change in patients undergoing carotid artery angioplasty and/or stent-supported angioplasty, and (b) to ascertain the time it takes for these changes to resolve.

NCT ID: NCT00597883 Completed - Stroke Clinical Trials

Neuropsychometric Outcome After Carotid Endarterectomy

CEA
Start date: March 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine how well patients undergoing carotid endarterectomy will perform on a battery of tests to assess brain function before and after surgery as compared to a control group of patients undergoing spine surgery. This study will serve to: (a) determine incidence of neurologic/neuropsychometric change in patients undergoing carotid artery surgery, and (b) to ascertain the time it takes for these changes to resolve.

NCT ID: NCT00592761 Completed - Stroke Clinical Trials

Treatment of Dysphagia Using the Mendelsohn Maneuver

Start date: July 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The primary goal of the investigation is to determine the effects of the Mendelsohn maneuver on the physiology of the swallow in individuals who have suffered a stroke and exhibit signs of pharyngeal dysphagia.