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Stroke clinical trials

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NCT ID: NCT00253097 Active, not recruiting - Clinical trials for Myocardial Infarction

The Post Stroke Preventive Trial (PREVENT). A RCT Nested in a Cohort Study

PREVENT
Start date: December 2005
Phase: N/A
Study type: Interventional

Patients with a diagnosis of stroke or TIA, who are already included in the RIALTO-cohort study are asked to participate in a RCT after discharge from hospital. Patients in the intervention group will receive four visits by a study nurse with the aim of controlling the patient's hypertension, reducing risk factors like tobacco smoking and obesity, and motivating the patient to physical activity and to a healthy diet.Patients in the control group will receive the usual treatment. This study is aimed at testing the hypothesis, that Primary outcome: the blood pressure lowering will be greater in the intervention group Secondary outcomes: the blood pressure will be lower in the intervention group and the number of patients who have stopped smoking will be greater in the intervention group The number of obese patients who have reduced their BMI will be greater in the intervention group The number of patients with a Rankin Scale<3 who are physically active for four hours a week will be greater in the intervention group Time to recurrent stroke, MI and death will be longer in the intervention group Outcomes are measured by follow up visit one and two years after inclusion in the study Expected Total Enrollment: 342 in the RCT, 1200 in the cohort Study Start: 011205 (PREVENT) Study Completion: January 2009(PREVENT), September 2013 (RIALTO Cohort study)

NCT ID: NCT00227461 Active, not recruiting - Stroke Clinical Trials

Levetiracetam (Keppra) to Improve Chronic Aphasia in Post-stroke Patients.

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The study investigates the possibility that levetiracetam may improve the symptoms of chronic post-stroke aphasia.

NCT ID: NCT00204113 Active, not recruiting - Stroke Clinical Trials

Control of Unsupported Paraplegic Standing

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

The study will investigate the feasibility of using functional electrical stimulation (FES) of the calf muscles of paraplegic subjects to assist in posture stabilisation during standing. We aim to achieve postural stability by combining controlled FES of the lower-limb muscles with the voluntary motor control skills of the intact upper body.

NCT ID: NCT00201461 Active, not recruiting - Stroke Clinical Trials

Evaluation of the STARFlex® Septal Closure System in Patients With a Stroke or TIA Due to the Possible Passage of a Clot of Unknown Origin Through a Patent Foramen Ovale (PFO)

Start date: June 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of the study is to determine whether the STARFlex® septal closure system will safely and effectively prevent a recurrent embolic stroke/transient ischemic attack (TIA) and mortality in patients with a PFO and to demonstrate superiority of the STARFlex® device compared to best medical therapy.

NCT ID: NCT00197509 Active, not recruiting - Clinical trials for Cerebrovascular Accident

Sit-to-Stand Training for Survivors of Stroke in a Long-Term Care Setting

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if providing training using a Sit-to-Stand protocol for residents of Long-Term Care Facilities who have had a stroke will increase their independence in performing Sit-to-Stand.

NCT ID: NCT00172146 Active, not recruiting - Stroke Clinical Trials

Influences of Cane Use on Voluntary Forward Stepping Movement and Associated Attentional Demands in Hemiplegic Patients

Start date: August 2002
Phase: N/A
Study type: Observational

The purpose of this study was to examine the influence of cane use on the movement, kinetics, and associated attentional demands of performing a voluntary forward stepping movement in patients with stroke and age-matched healthy adults.

NCT ID: NCT00170716 Active, not recruiting - Stroke Clinical Trials

Safety and Effectiveness of Cortical Stimulation in the Treatment of Stroke Patients With Upper Extremity Hemiparesis

EVEREST
Start date: September 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of cortical stimulation delivered concurrent with rehabilitation activities to enhance motor recovery in patients suffering from hemiparesis affecting the upper extremity following a stroke.

NCT ID: NCT00167076 Active, not recruiting - Stroke Clinical Trials

Clinical Applications and Evaluations of A Portable In-Shoe Plantar Pressure Monitoring and Biofeedback Gait System for Ambulation Training in Stroke Rehabilitation

Start date: August 1999
Phase: N/A
Study type: Observational

The purposes of this paper were to determine whether walking speed affected gait parameters and force impulse in patients with stroke or not, and if the changes varied in various foot regions.

NCT ID: NCT00167063 Active, not recruiting - Stroke Clinical Trials

Falls in Stroke Patients After Hospital Discharge: Prevalence and Risk Factors

Start date: August 1999
Phase: N/A
Study type: Observational

The purposes of this study are: (1) to investigate the incidence and causes of falls of stroke patients residing in Taipei City and Taipei county after their discharge from the National Taiwan University Hospital, (2) to investigate the relationship between clinical manifestations of stroke patients before their hospital discharge and their incidence of falls after hospital discharge, and (3) to identify the risk factors for stroke patients who frequently fall after hospital discharge.

NCT ID: NCT00167037 Active, not recruiting - Stroke Clinical Trials

Fast Stepping in Stroke Patients for Fall Prediction and Prevention:Control Mechanisms and Clinical Implications

Start date: August 1999
Phase: N/A
Study type: Observational

The purpose of this study was to compare the balance strategy, as well as center of pressure (COP) trajectory and parameters between healthy adults and patients with hemiplegia in response to slow- and fast-speed waist- pulling perturbations in forward, left, right, and backward directions.