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Stroke clinical trials

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NCT ID: NCT00847860 Completed - Stroke Clinical Trials

Cilostazol Verse Asprin for Vascular Dementia in Poststroke Patients With White Matter Lesions

CAVAD
Start date: March 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of PDE-3 inhibitor, cilostazol, in prevention and treatment of vascular dementia, in those with brain white matter lesions and vascular risk factors.

NCT ID: NCT00847704 Terminated - Stroke Clinical Trials

Clinic-Based AMES Treatment of Stroke

Start date: April 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The hypothesis of this study is that chronic stroke survivors, more than one year post-stroke, with a motor problems in the lower extremity will be able to walk and move the affected leg better after 30 treatments with a new robotic therapy device, the AMES device. The device rotates the ankle while vibrators stimulate the tendons attached to muscles that move the ankle. Testing will be done before, during and after the treatments to determine response to the therapy.

NCT ID: NCT00846924 Active, not recruiting - Stroke Clinical Trials

30-Day Cardiac Event Monitor Belt for Recording Atrial Fibrillation After a Cerebral Ischemic Event

EMBRACE
Start date: May 2009
Phase: N/A
Study type: Interventional

Atrial fibrillation is the most common cardiac cause of ischemic stroke. Detecting atrial fibrillation after a stroke or TIA is critical because highly effective secondary stroke prevention therapy is available for individuals who are recognized to have atrial fibrillation. However, atrial fibrillation is likely under-diagnosed after stroke and TIA because atrial fibrillation is often difficult to detect as it is frequently paroxysmal and asymptomatic, and patients do not routinely undergo prolonged screening. The purpose of this study is to determine the diagnostic yield of a novel 30-day cardiac event monitor compared to a repeat 24-hour Holter monitor for detecting occult paroxysmal atrial fibrillation in patients with a recent ischemic stroke or TIA of undetermined etiology after completion of a standard clinical stroke work-up (including an initial negative Holter monitor.)

NCT ID: NCT00845455 Completed - Stroke Clinical Trials

Personality Type as a Predictor to Develop Depression and Reduction in Quality of Life Among Stroke Survivals.

TPQ BDI SSQOL
Start date: November 2007
Phase: N/A
Study type: Observational

Personality type as a predictor to develop depression and reduction in quality of life among stroke survivals.

NCT ID: NCT00844870 Completed - Stroke Clinical Trials

Exploring New Approaches in Reaching Behavior Post Stroke

Start date: April 2007
Phase: N/A
Study type: Interventional

After 4 weeks of training the hypothesis that the more natural training program would yield greater functional changes was proven correct.

NCT ID: NCT00843765 Completed - Stroke Clinical Trials

Efficiency Study of Traditional Chinese Medicine (TCM) Versus Western Medicine (WM) on Ischemic Stroke

Start date: December 2007
Phase: N/A
Study type: Interventional

Complex project of Traditional Chinese Medicine (TCM) with Western Medicine (WM) project under stroke unit mode contrast,assuming that the efficiency of TCM on early rehabilitation and secondary prevention of ischemic stroke is same or better than that of WM.

NCT ID: NCT00843427 Completed - Stroke Clinical Trials

fMRI of Language Recovery Following Stroke in Adults

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

The purpose of this study is to test the effectiveness of constraint-induced aphasia therapy.

NCT ID: NCT00840671 Completed - Stroke Clinical Trials

Combined Treatment With Alteplase (Rt-PA) and Cerebrolysin® in Acute Ischemic Hemispheric Stroke

CERE-LYSE-1
Start date: October 2005
Phase: Phase 3
Study type: Interventional

It should be shown that Cerebrolysin in combination with Alteplase, the medication that should recover the blood flow through the brain, is an effective and save medication to treat ischeamic stroke.

NCT ID: NCT00839670 Terminated - Stroke Clinical Trials

Light Constraint Induced Therapy Experiment

LICITE
Start date: February 2009
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to compare the effect of a modified constraint induced therapy to the treatment described originally by Taub et al.. This study will determine if LICITE will lead to similar improvements than the original described method.

NCT ID: NCT00839657 Completed - Stroke Clinical Trials

Clarification of Optimal Anticoagulation Through Genetics

COAG
Start date: September 2009
Phase: Phase 3
Study type: Interventional

Individuals taking warfarin often need frequent dose changes as the international normalized ratio (INR) gets too high or too low which could result in a higher risk of thromboembolism, bleeding and early discontinuation of a highly useful therapy. This study will compare two approaches to warfarin dosing to examine the utility of using genetic information for warfarin dosing.