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Stroke clinical trials

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NCT ID: NCT00866112 Completed - Stroke Clinical Trials

A Randomized Exercise Trial for Wheelchair Users

Start date: May 2008
Phase: N/A
Study type: Interventional

People with mobility disabilities are at greater risk than the general population for incurring health problems. Many of these conditions are preventable through behavior and lifestyle changes such as exercise and physical activity. Recent evidence suggests that people with disabilities experience the same physiologic response to exercise as the general population. Nonetheless, nearly three-fourths of those with disabilities report being entirely sedentary or not active enough to achieve health benefits. Despite some knowledge of issues that limit physical activity among this population, few studies have investigated methods for promoting physical activity adoption among people with disabilities, including wheelchair users. The purpose of this study is to test the effectiveness of a behavioral intervention to promote physical activity adoption over 6 months and maintenance of physical activity over another 6 months by community-dwelling manual wheelchair users.

NCT ID: NCT00864708 Terminated - Stroke Clinical Trials

Enhancing Function Using the RF Microstimulator Gait System Following Stroke 2008

Start date: December 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate new Technology for recovery of ankle walking function after stroke.

NCT ID: NCT00863967 Active, not recruiting - Stroke Clinical Trials

Early Detection of Arteriosclerosis

Start date: October 2003
Phase: N/A
Study type: Observational

Arteriosclerosis is a common chronic disease with well known risk factors like diabetes mellitus, hypertension, dyslipidemia, adipositas and smoking, leading to severe complications like myocardial infarction, stroke or peripheral arterial occlusive disease. In addition to life-style factors there is also a genetic predisposition to develop complicated atherosclerosis. Objective: Improve individual risk prediction by clinical phenotyping and genotyping.

NCT ID: NCT00862160 Recruiting - Clinical trials for Coronary Artery Disease

Incidence of Acute Cerebrovascular Events Using Either Minimized or Standard Cardiopulmonary Bypass Circuit

ROCsafeTM
Start date: April 2009
Phase: Phase 4
Study type: Interventional

The prospective, randomized, two centre study investigates acute cerebrovascular events during extracorporal circulation and the early post operative outcome when using either the minimized cardiopulmonary bypass circuit (ROCsafeTM) or a standard cardiopulmonary bypass circuit in patients undergoing coronary artery bypass grafting.

NCT ID: NCT00861133 Recruiting - Cryptogenic Stroke Clinical Trials

Cryptogenic Stroke Study

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Sleuth Implantable Loop Recorder will enhance detection of latent atrial fibrillation in patients after cryptogenic stroke.

NCT ID: NCT00861081 Completed - Stroke Clinical Trials

Intervention to Enable Stroke Survivors in Los Angeles County Hospitals to "Stay Within the Guidelines"

SUSTAIN
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to test a newly developed outpatient care intervention called SUSTAIN (Systematic Use of Stroke Averting Interventions) for improving delivery of stroke preventive services at Los Angeles County hospitals and to measure the costs of running such an intervention.

NCT ID: NCT00860366 Completed - Clinical trials for Acute Ischemic Stroke

Efficacy Study of Combined Treatment With Uric Acid and rtPA in Acute Ischemic Stroke

Urico-Ictus
Start date: June 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether the combined treatment with Uric Acid and rtPA is superior to rtPA alone in terms of clinical efficacy in acute ischemic stroke patients treated within the first 4.5 hours of symptoms onset.

NCT ID: NCT00860210 Completed - Stroke Clinical Trials

Pilot Study Assessing the Feasibility of Treating Foot Drop With the Neurostep™ System.

Start date: October 2007
Phase: Phase 1
Study type: Interventional

This pilot feasibility study is assessing the safety and technical performance of the Neurostep™ System for the restoration of independent gait in subjects with gait disorder (i.e. foot drop) secondary to a CNS lesion (e.g. stroke).

NCT ID: NCT00859885 Recruiting - Stroke Clinical Trials

International PFO Consortium

Start date: September 8, 2008
Phase: N/A
Study type: Observational

The prevalence of patent foramen ovale (PFO) is about 25% in the general population and approximately 40% in patients who have ischemic stroke of unknown cause (cryptogenic stroke). Given the large number of asymptomatic patients, no primary prevention is currently recommended. On the contrary, secondary prevention is very important. Prospective studies have shown that antithrombotic treatment (ATT) with aspirin or warfarin appears to negate the risk of recurrent stroke associated with a PFO. Patients with spontaneous or large right-to-left shunts (RLS), those with a coinciding atrial septal aneurysm (ASA) or multiple ischemic events prior to the PFO diagnosis may still be at increased risk of stroke recurrence despite ATT. Percutaneous device closure (PDC) is a challenging alternative to ATT. Several studies reported 0% to 3.4% annual recurrence rates of stroke or TIA in patients treated by PDC. To date, there is no data from randomized controlled trials (RCT) comparing the risk of stroke recurrence after PDC with that under ATT only. The results from ongoing RCTs are not to be awaited in the near future, mainly due to low enrolment and event rates. Alternative data-gathering strategies such as multicenter registries are needed to overcome the low recruitment rates. The aim of the present study is to compare the risk of recurrent stroke and TIA in patients with PFO and otherwise unexplained stroke who undergo PDC or receive ATT.

NCT ID: NCT00859014 Completed - Ischemic Stroke Clinical Trials

Safety/Feasibility of Autologous Mononuclear Bone Marrow Cells in Stroke Patients

Start date: January 2009
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to find out if bone marrow treatment (bone marrow aspiration and infusion of stem cells) can be safely used in adults who have recently (within 24-72 hours)suffered an acute ischemic stroke.