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Ischemic Attack, Transient clinical trials

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NCT ID: NCT01317849 Withdrawn - Stroke Clinical Trials

China Stroke Secondary Prevention Trial

CSSPT
Start date: July 2011
Phase: N/A
Study type: Interventional

The CSSPT study is a multi-center, randomized, double blinded, placebo-controlled secondary stroke prevention trial in China to determine whether the addition of folic acid and vitamin supplements will reduce recurrent stroke events and other combined incidence of recurrent vascular events and vascular death.

NCT ID: NCT01284933 Completed - Stroke Clinical Trials

Carotid Plaque Imaging in Acute Stroke

CAPIAS
Start date: February 2011
Phase:
Study type: Observational

The purpose of this study is to determine the frequency, characteristics, and consequences of vulnerable carotid artery plaques ipsilateral to an acute ischemic stroke or TIA in the territory of the internal carotid artery.

NCT ID: NCT01272843 Not yet recruiting - Clinical trials for Transient Ischemic Attack

Physiological Magnetic Resonance Imaging (MRI) to Improve Carotid Endarterectomy Outcomes

Start date: February 2011
Phase: N/A
Study type: Observational

The carotid arteries are blood vessels in the neck that supply blood to the brain. Carotid stenosis disease is defined as a narrowing of these arteries due to the build up of plaque. The plaque material can also break off and move into the brain. The resulting blockage of blood supply to a portion of the brain is what causes 80% of all strokes. One treatment option is to have surgery on the carotid artery and remove the plaque. This procedure is called a carotid endarterectomy (CEA). There is evidence that proves CEA reduces the risk of stroke. The objective of this research project is to determine who is most likely to benefit from CEA surgery.

NCT ID: NCT01252875 Completed - Ischemic Stroke Clinical Trials

Treat Stroke to Target

TST
Start date: March 15, 2010
Phase: N/A
Study type: Interventional

The aim of this study is the evaluation of two usual care strategies after stroke or TIA : achieved target LDL-C of 100 mg/dL (+/-10 mg/dL) or less than 70 mg/dL. Investigators will use the statin and titrate the dosage to achieve the target assigned by randomization in monotherapy or in combination with ezetimibe or other drugs. The primary end-point is the occurrence of recurrent non fatal stroke, non fatal MI, and vascular death in each group. 3760 patients will be recruited and followed for eight and a half years maximum.

NCT ID: NCT01115660 Completed - Ischemic Stroke Clinical Trials

Stroke Education Intervention Trial - Pilot

AVAIL II
Start date: January 2010
Phase: N/A
Study type: Interventional

The objectives of the trial of a medication-coach program for patients with stroke or transient ischemic attack are to pilot test the study design, the intervention components and the data collection forms and refine them for a larger trial whose goal will be to improve long-term adherence to stroke prevention medications.

NCT ID: NCT01100385 Completed - Stroke Clinical Trials

TomVasc - Vascular Effects of Tomato Extract

TomVasc
Start date: February 2010
Phase: N/A
Study type: Interventional

Does tomato extract improve blood vessel function in healthy people and people with cardiovascular disease? Atherosclerosis ('furring' of the arteries) affects the functioning of blood vessels, narrowing and eventually blocking them, causing conditions like heart attack and stroke. The Mediterranean diet, which is rich in tomatoes and tomato-based products, has been shown to be associated with a reduced risk of blood vessel damage. In this double blind, placebo-controlled randomised study, the investigators will investigate whether a food supplement containing a standardised extract of tomato improves blood vessel function in both healthy people (aged 40-80), and people with a history of cardiovascular disease. The food supplement is on sale to the public, and the investigators are testing the standard dose. Approximately 72 people will take part at the Clinical Pharmacology Unit at the ACCI Building, Cambridge University Hospitals NHS Trust. After they have passed screening tests, participants will be allocated by chance to receive either the tomato extract product (Ateronon), or a matching placebo (a dummy capsule with no active ingredients), which they will take once a day for 8 weeks. At the beginning and end of the treatment period, the investigators will test blood vessel stiffness using an ECG machine and external probe. The investigators will also measure forearm blood flow, which involves infusing 3 separate agents that affect how the lining of the blood vessel wall works, and helps to assess whether this is affected by the study treatment. Blood tests will also be used to look at how the food supplement is working and its effects on cholesterol and markers of inflammation. Including the screening period, and a follow-up telephone call two weeks after the end of treatment, participants will be in the study for 14 weeks.

NCT ID: NCT01097967 Active, not recruiting - Ischemic Stroke Clinical Trials

Sleep Disordered Breathing in Transient Ischemic Attack (TIA)/Ischemic Stroke and Continuous Positive Airway Pressure (CPAP) Treatment Efficacy

SAS-CARE
Start date: July 2010
Phase: Phase 4
Study type: Interventional

The study aims to observe the short term effect (3-month) of sleep disordered breathing (SDB) on cardiovascular parameters, heart rate variability, endothelial function and surrogate markers of atherosclerosis after acute cerebrovascular events (ACE). The long-term effect (6-24-month) of Continuous Positive Airway Pressure (CPAP) on clinical vascular outcome, cardiovascular parameters, evolution of surrogate of atherosclerosis heart rate variability and endothelial function after ACE is observed over 24 months. A preventive effect of CPAP therapy on cerebro-vascular events in patients with moderate-severe obstructive SDB without sleepiness after ictus or transient ischaemic attack will be evaluated.

NCT ID: NCT01071408 Completed - Ischemic Stroke Clinical Trials

Trial of a Secondary Stroke Prevention Program

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an outpatient program can reduce the risk of recurrent stroke.

NCT ID: NCT01038375 Completed - Blood Pressure Clinical Trials

Tailored Interventions to Improve Hypertension Management After Stroke or Transient Ischemic Attack (TIA)

TIMSII
Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine the effectiveness of interventions to improve adherence to medication and healthier lifestyle choices on blood pressure over a 6 month period in a group of people at high risk for recurrent stroke events. The participants have already had a stroke or TIA, and have uncontrolled blood pressure, as well as problems with memory and problem-solving, or miss taking medications, or who do not believe in the effectiveness of their medications. Interventions focus on motivational interviewing, adherence counseling with memory cuing, and self-monitoring of blood pressure.

NCT ID: NCT01027273 Completed - Clinical trials for Transient Ischemic Attack

Prevent Return of Stroke Study

Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if a peer-led stroke recurrence prevention intervention, versus usual care, will help reduce risk factors for recurrent strokes among adults in Harlem.