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Stroke clinical trials

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NCT ID: NCT01794182 Completed - Ischemic Stroke Clinical Trials

Glyburide Advantage in Malignant Edema and Stroke - Remedy Pharmaceuticals

GAMES-RP
Start date: June 13, 2013
Phase: Phase 2
Study type: Interventional

This is a randomized, multi-center, prospective, double blind study. The primary objective is to assess the efficacy and safety of glyburide (RP-1127) compared to placebo in participants with a severe anterior circulation ischemic stroke who are likely to develop malignant edema.This objective will be addressed by comparing the proportion of glyburide treated particpants and placebo treated participants with a Day 90 modified Rankin Scale (mRS) ≤ 4 without decompressive craniectomy (DC). The secondary objective is to assess the efficacy of RP-1127 compared to placebo in participants with a severe anterior circulation ischemic stroke who were likely to develop malignant edema.

NCT ID: NCT01792349 Recruiting - Stroke Clinical Trials

Increasing Physical Activity in Stroke Survivors Using STARFISH

Start date: February 2013
Phase: N/A
Study type: Interventional

There is good evidence of the effectiveness of regular physical activity in the primary and secondary prevention of stroke. STARFISH is a smartphone-based application designed as a behavioural change intervention to encourage the user to become more physically active. The study will investigate if using STARFISH for 6 weeks can increase physical activity in people after stroke. Subjects will be randomised to the STARFISH intervention or a control group. Control subjects will not have access to their daily activity count.

NCT ID: NCT01790997 Completed - Clinical trials for Acute Ischemic Stroke

Efficacy of DLBS1033 in Patients With Acute Ischemic Stroke

Start date: May 2012
Phase: Phase 3
Study type: Interventional

This is a 3-arm, prospective, randomized, double-blind, and controlled clinical study, with 3 months of treatment to evaluate efficacy of DLBS1033 in bleeding profile and clinical outcome in patients with acute ischemic stroke compared with aspirin and clopidogrel, as active controls.

NCT ID: NCT01790880 Completed - Stroke Clinical Trials

Enhancing Written Communication in Persons With Aphasia

Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether a computerized speech-language treatment delivered by a virtual therapist (Oral Reading for Language in Aphasia (ORLA) + Writing) results in improved written communication skills of study participants with aphasia (i.e., difficulty with the comprehension and expression of spoken and written language).

NCT ID: NCT01789853 Completed - Stroke Clinical Trials

Very Intensive Early Walking in Stroke

VIEWS
Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the efficacy of intensive locomotor interventions early post stroke. An intensive locomotor training (LT) program will be compared to an active control, conventional physical therapy. It is proposed that an early and intensive stepping paradigm that is not typically employed early in physical therapy will lead to superior outcomes and improved community mobility. A randomized, blinded, controlled trial will test subjects with moderate to severe locomotor dysfunction in individuals post-stroke to compare walking-related outcomes after intensive gait training (including treadmill, overground, stair training, and skilled walking training) to outcomes after conventional physical therapy.

NCT ID: NCT01787877 Not yet recruiting - Clinical trials for Cerebrovascular Accident

Inflammatory Biomarkers as Tool in Diagnosis and Management of Patients With Ischemic Stroke

Start date: February 2013
Phase: N/A
Study type: Observational

Stroke represents the third commonest cause of death after heart disease and all types of cancer combined, and is the leading cause of long-term permanent disability among adults. Recombinant tissue plasminogen activator (tPA) is currently the only safe medical treatment for acute ischemic stroke but only a small fraction of patients are eligible for a thrombolysis treatment. Current guidelines on thrombolysis post stroke with tPA exclude its uses beyond 3 hours after stroke onset and when time of onset is unknown thus excluding many patients from potentially beneficial treatment. For an appropriate triage and management of patients, it is essential to improve imaging techniques beyond a simple CT scan. Perfusion computed tomography (PCT), currently considered as an investigational technique, permits a quantitative determination of the cerebral perfusion within the brain. It helps distinguish salvageable ischemic penumbra from irreversibly infarcted core in acute stroke patients. This technique has therefore the potential to select patients who are most likely to benefit from thrombolysis with tPA, can be used to predict the benefit after thrombolysis and determine the suitability for other therapeutic interventions. In patients with a primary diagnosis of TIA, PCT would help to identify possible persistent cerebral ischemia but also provide important information for rapid instigation of prophylactic strategies. The diagnosis and management of patients with ischemic stroke and TIA is challenging and is primarily based on clinical assessment in conjunction with neuroimaging. Development of specific molecular biomarkers as additional tools to support a clinical diagnosis, exclude common stroke mimics such as migraine or epileptic seizures, identify patients at risk of disease, and help guide patient treatment by predicting complications following t-PA treatment would be of great value.

NCT ID: NCT01786785 Completed - Clinical trials for Acute Arterial Ischemic Stroke

Optical Measurement of Cerebral Hemodynamics in Children With Acute Arterial Ischemic Stroke

Start date: February 2012
Phase:
Study type: Observational

Acute ischemic stroke affects roughly 1 in 50,000 children every year and is one of the top ten causes of death in children. Currently, caregivers lay the affected child flat in hopes of increasing blood flow to the brain and reducing the volume of the brain which is damaged. However, there are currently no techniques to measure brain blood flow at the child's bedside and indicate if this treatment is effective. We will probe brain blood volume, oxygen saturation, and flow with red light to determine the efficacy of this intervention.

NCT ID: NCT01786486 Completed - Stroke Clinical Trials

AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol

ACPR
Start date: August 2009
Phase:
Study type: Observational [Patient Registry]

The objective of the AMPLATZER Cardiac Plug (ACP) Registry Long Term Follow-up study is to evaluate long term performance of the ACP in closure of the Left Atrial Appendage (LAA) in subjects with nonvalvular atrial fibrillation and assess adverse events up to two (2) or more years post implant.

NCT ID: NCT01784796 Completed - Stroke Clinical Trials

Mindful Hearts Study: Mindfulness to Reduce Stress

Start date: July 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how a stress reduction program, called Mindfulness Based Stress Reduction (MBSR), compared to a health education program, improves well being and reduces the risk of heart disease in women Veterans. Recruitment completed.

NCT ID: NCT01783639 Completed - Stroke Clinical Trials

Safety and Performance Evaluation of WIRION™ EPD in Patients Undergoing Carotid Artery Stenting

WISE
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the safety and performance of WIRION™ EPD in patients undergoing carotid artery stenting to a performance goal based on an analysis of the results of previous US IDE carotid stenting with embolic protection studies