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Stroke clinical trials

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NCT ID: NCT00552916 Recruiting - Stroke Clinical Trials

Functional Electrical Stimulation (FES) Assisted Walking: Enhancement of Walking Function After Stroke

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if a form of exercise,known as electrical stimulation can improve walking function and other important health outcomes. The hypothesis is that electrical stimulation can enhance the ability to walk for stroke survivors who are unable to walk on their on their own.

NCT ID: NCT00548223 Completed - Stroke Clinical Trials

The Secondary Prevention Trial for Ischemic Stroke With DengzhanShengmai Capsule

SPIRITDZSM1
Start date: December 2007
Phase: Phase 4
Study type: Interventional

In order to observe the secondary preventive effect of the Dengzhanshengmai capsule on ischemic stroke, the investigators hold the large randomized control trial (RCT). 3143 subjects are included in 83 clinical research centers all over China. The subjects are randomly grouped into two groups. The basic therapy included antiplatelet aggregation, stroke health education, management of blood pressure, blood lipid and blood glucose, etc. The treating group will take the compound Chinese Medicine Deng Zhan Sheng Mai capsule and the contrast group will take the placebo for twelve months. Then all of the subjects are visited on the 30th, 90th, 180th, 360th day after inclusion. The recurrence of stroke, cardiovascular events, and peripheral arterial events are observed.

NCT ID: NCT00547950 Not yet recruiting - Ischemic Stroke Clinical Trials

A Multiple-Centered, Prospective Cohort Study: the Second Prevention Trial for Ischemic Stroke With Deng Zhan Sheng Mai Capsule(SPIRIT—DZSM-2)

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

In order to observe the influence of the Dengzhan Shengmai Capsule on the endpoint of patients with ischemic stroke, we hold the multi-centered prospective cohort study. From November 2007 to December 2009, 12000 subjects are included in 200 clinical research centers all over China. The subjects naturally formed two cohorts based on taking Dengzhan Shengmai capsule or not. The basic therapy included antiplatelet aggregation , stroke health education, management of blood pressure, blood lipid and blood glucose, etc. Then all of the subjects are visited on the 360th day after inclusion. The recurrence of stroke, cardiovascular events, and peripheral arterial events are observed.

NCT ID: NCT00547690 Terminated - Stroke Clinical Trials

Acupuncture in Stroke Rehabilitation

Start date: April 2003
Phase: Phase 2
Study type: Interventional

The primary purpose of the study is to examine the effect of acupuncture treatment when combined with strength training on the motor functional recovery of stroke survivors

NCT ID: NCT00544622 Completed - Stroke Clinical Trials

Structured Stroke Management Improves Outcome at 6 Months

Start date: January 2002
Phase: N/A
Study type: Interventional

Background/Aim of the study: To further reduce the 6 months stroke morbidity and mortality in a high volume stroke hospital and to compare the results with national and international data. Methods: 204 consecutive stroke patients are analyzed in a prospective study in a single center teaching institution. The intervention consists of a structured therapeutic chain of 290 collaborating GPs, a standardised acute hospital proceeding overlapping with an early integrated neurovascular rehabilitation within the same institution. Primary endpoints include death and dependence at 6 months, secondary endpoints are the length of hospital stay (LOS) and the quantitative analysis of physical and psychosocial impairments. The data are directly compared with the same endpoints of the Swiss subgroup of the international stroke trial (IST).

NCT ID: NCT00542802 Recruiting - Stroke Clinical Trials

Levetiracetam Versus Carbamazepine in Post-Stroke Late Onset Crisis

EpIc
Start date: September 2007
Phase: Phase 3
Study type: Interventional

The principal purpose of the study is to determine the efficacy and safety of Levetiracetam versus Carbamazepine, intended as the number of patients free from crisis during the whole period of treatment, in patients affected by post stroke late onset crisis.

NCT ID: NCT00542256 Completed - Clinical trials for Cerebrovascular Accident

tDCS and Physical Therapy in Stroke

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

The purpose of this study is to determine whether a painless and noninvasive procedure called transcranial direct current stimulation (tDCS) combined with a method of physical therapy called constraint-induced movement therapy improves motor function in patients with chronic stroke. Research in healthy subjects has shown that when tDCS is combined with motor learning tasks, there is an increase in learning as compared to motor learning tasks only. The tDCS procedure sessions will be compared to sham (fake) procedure sessions, which is also called placebo stimulation. This study is double blind, which means neither the subjects nor researchers analyzing motor function will know if participants are receiving real tDCS stimulation or placebo. Only the person performing the procedure will know which one participants are receiving. Only by comparing the tDCS procedure to a sham (placebo) procedure can we understand if the tDCS actually improves motor function. We hypothesize that tDCS will enhance the effects of constraint-induced movement therapy on motor recovery in chronic stroke patients.

NCT ID: NCT00540527 Completed - Stroke Clinical Trials

Local Versus Systemic Thrombolysis for Acute Ischemic Stroke (SYNTHESIS)

Start date: January 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether intra-arterial rt-PA within 6 hours from an ischemic stroke onset, compared with intravenous infusion of the same drug within 3 hours, increases the proportion of independent survivors at 3 months.

NCT ID: NCT00537264 Completed - Stroke Clinical Trials

A Comparison of Computerised Versus Interviewer-administered Approach for Assessing Health-related Quality of Life

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

The aim of this study is to compare a multimedia, computerised approach vs. interviewer administration of health-related quality of life (HRQoL) instruments.

NCT ID: NCT00535197 Completed - Stroke, Acute Clinical Trials

Autologous Bone Marrow Stem Cells in Ischemic Stroke.

Start date: September 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to determine the safety and tolerability of an autologous CD34+ subset bone marrow stem cell infusion into the middle cerebral artery in patients who have suffered acute total or partial anterior circulation syndrome (TACS/PACS).