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Acute Stroke clinical trials

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NCT ID: NCT01501773 Completed - Acute Stroke Clinical Trials

Intravenous Autologous Bone Marrow-derived Stem Cells Therapy for Patients With Acute Ischemic Stroke

Start date: October 2008
Phase: Phase 2
Study type: Interventional

A multi-centric initiative to study safety,feasibility and efficacy of using intravenous autologous bone marrow mononuclear cells(BMMC) in patients with acute ischemic stroke.This phase of study is visualised as phase 2 study and will aim to determine dose response gradient of stem cell therapy and to explore if there is favorable risk to benefit ratio for autologous stem cell therapy in patient with acute ischamic stroke.

NCT ID: NCT01442766 Withdrawn - Acute Stroke Clinical Trials

Donepezil Trial for Motor Recovery in Acute Stroke

Start date: November 2011
Phase: Phase 1/Phase 2
Study type: Interventional

AIMS: To establish: 1) whether motor deficits in acute stroke improve more in patients taking donepezil, relative to placebo, for 12 weeks; 2) whether brain functional MRI changes as a result of donepezil after 12 weeks.

NCT ID: NCT01399762 Recruiting - Acute Stroke Clinical Trials

International Multicenter Registry for Mechanical Recanalization Procedures in Acute Stroke

ENDOSTROKE
Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of the Endostroke Registry is to gather information on predictors of good or poor clinical outcome following mechanical recanalization therapies for acute ischemic stroke.

NCT ID: NCT01382862 Completed - Acute Stroke Clinical Trials

PHANTOM-S: The Pre-Hospital Acute Neurological Therapy and Optimization of Medical Care in Stroke Patients - Study

PHANTOM-S
Start date: May 2011
Phase: Phase 2
Study type: Interventional

The purpose of this prospective study in acute ischemic stroke patients is to compare alarm-to-needle time during randomly allocated periods with and without availability of a specially staffed ambulance equipped with computed tomography (CT) and point-of care diagnostics. The investigators hypothesize that compared to regular care the investigators will reduce alarm-to-needle time by a minimum of 20 minutes by implementation of the stroke emergency mobile unit.

NCT ID: NCT01282242 Active, not recruiting - Acute Stroke Clinical Trials

MR WITNESS: A Study of Intravenous Thrombolysis With Alteplase in MRI-Selected Patients

MR WITNESS
Start date: January 2011
Phase: Phase 2
Study type: Interventional

This study was jointly developed and is jointly led by investigators at Massachusetts General Hospital and the intramural division of NINDS. We are doing this research study to find out if Activase ® (also called alteplase or rt-PA) can safely be given to people with an acute ischemic stroke when their stroke onset was not witnessed making them ineligible for standard thrombolytic (clot busting) therapy. We also want to find out if rt-PA can help people recover better from their stroke. The purpose of this study is to: 1) see if it is safe to give intravenous (IV) rt-PA to people with unwitnessed stroke but with MRI evidence of early ischemic stroke, 2) see if rt-PA is effective if given to people who are selected for treatment based on MRI evidence of an early stroke, and 3) get information about this new MRI diagnostic methods for guiding stroke treatment.

NCT ID: NCT01265043 Completed - Acute Stroke Clinical Trials

A Randomized Clinical Trial of Oral Health Promotion Interventions Among Patients After Stroke

Start date: July 2008
Phase: Phase 4
Study type: Interventional

The main aim of this oral health intervention project is to compare the effect of providing 1) professional oral hygiene instruction alone versus 2) professional oral hygiene instruction plus adjunctive Chlorhexidine mouth rinse versus 3) professional oral hygiene instruction plus adjunctive assisted tooth brushing and Chlorhexidine mouth rinse, on the oral health condition, the general health condition and health-related quality of life (HRQoL) of patients with stroke who are receiving hospital-based rehabilitation. An additional aim is to assess potential longer term oral intervention-related health and HRQoL outcomes.

NCT ID: NCT01210729 Completed - Acute Stroke Clinical Trials

Mechanical Recanalization With Flow Restoration in Acute Ischemic Stroke

ReFlow
Start date: September 2010
Phase: Phase 2
Study type: Interventional

The objective of this study is to collect data on the use of the SOLITAIR FR device for treatment of acute ischemic stroke with large artery occlusion i.e. to investigate, whether the application of SOLITAIR is a safe and feasible method for interventional recanalization of large vessels with favorable patient outcome in acute stroke therapy.

NCT ID: NCT01177748 Completed - Acute Stroke Clinical Trials

Stroke Arrhythmia Monitoring Database

SAMBA
Start date: June 2010
Phase: N/A
Study type: Observational

Cardiac arrhythmia are frequently observed after stroke. They may on one hand be causative for the stroke mainly in case of atrial fibrillation but on the other hand present severe complications of the stroke. In addition, cardiac comorbidity as well as acute myocardial infarction are frequently found in acute stroke patients. Diagnostics to identify cardiac arrhythmia in the acute phase of stroke care thus have an important role not only for adjusting the correct secondary prevention but also to prevent cardiac complications potentially reducing morbidity and mortality. The aim of the SAMBA-Study is to systematically assess the prevalence of higher grade arrhythmias after stroke using a standardized reading of 72h telemetric monitoring in the first days after stroke onset. In addition, it evaluates different strategies to identify paroxysmal atrial fibrillation.

NCT ID: NCT01175525 Not yet recruiting - Acute Stroke Clinical Trials

Treatment of Acute Stroke With Cromolyn(Single Dose)

Start date: n/a
Phase: Phase 3
Study type: Interventional

Mastocytes were proven to have a central rule in their development of the lipoid plaque of the vascular system. Mastocytes also has an important role in the stabilisation of the plaque in the building of the brain barrier. Different animal studies show that the inhibition of the mastocyte activity decreases significantly the risk of secondary bleeding post ischaemic stroke.It was also shown that post stroke inflammation process was also blocked by the inhibition of mastocytes.Other studies showed up to 100% decrease in the brain barrier disruption and post stroke oedema, after treatment with mastocyte inhibitors. Cromolyn is a synthetic drug which has an anti-allergic effect by inhibition of the mastocytes. This drug is a well known,safe drug and is the main sub-substance that was used in the previously mentioned studies.

NCT ID: NCT01148602 Completed - Acute Stroke Clinical Trials

The CLOQS Trial - Countdown Lights to Optimize Quality in Stroke

CLOQS
Start date: June 2010
Phase: N/A
Study type: Interventional

To reduce door-to-needle times in acute stroke treatment. Using an organizational behaviour intervention (a large stopwatch), we will post a visual cue to remind all parties that "time is brain". We hypothesize that this simple visual cue will improve door-to-CT scan times and door-to-needle treatment times, and thus improve treatment response, and reduce adverse events.