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Ischemia clinical trials

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NCT ID: NCT01546636 Completed - Cerebral Ischemia Clinical Trials

The Effect of Ventilation on Cerebral Oxygenation in the Sitting Position

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

The aim of this clinical investigation is to determine the effect of intraoperative ventilation on cerebral oxygen saturation in patients undergoing arthroscopic shoulder surgery in the beach chair position (BCP)

NCT ID: NCT01541163 Recruiting - Heart Diseases Clinical Trials

Heart and Ischemic STrOke Relationship studY

HISTORY
Start date: September 2010
Phase: N/A
Study type: Observational

Although cardio-embolic etiology of ischemic stroke (IS) is largely respected, there is still no clear recommendation for routine complex cardiological examination in all IS patients. Using complex cardiological examination the investigators expect: 1. more accurate detection of patients with concomitant heart disease (cardiac rhythm disorder, valve disorders, acute coronary syndrome, cardiac thrombus and myxoma, atrial and ventricle septum defects) 2. higher number of etiologically determinated IS, which is crucial for accurate secondary prevention.

NCT ID: NCT01531946 Completed - Clinical trials for Ischemic Attack, Transient

Acute MRI in Transient Ischemic Attack

Start date: January 2012
Phase:
Study type: Observational

The purpose of this study is to detect acute ischemic lesions in patients admitted with symptoms of transient ischemic attack (TIA). Diffusion weighted Imaging (DWI) is today one of the best ways to detect ischemic lesions after TIA. The problem is that this only gives the diagnosis in 30% of the cases. It is possible that the addition of Arterial spin labeling (ASL) perfusion imaging and diffusion tensor imaging will make it possible to give a more accurate diagnosis.

NCT ID: NCT01528462 Completed - Stroke Clinical Trials

Sleep Disorders Managed and Assessed Rapidly in Transient Ischemic Attack (TIA) and In Early Stroke

SMARTIES
Start date: October 2011
Phase:
Study type: Observational

The aim of the investigators was to determine whether the immediate management of any detected sleep disorders can improve outcomes in patients who have had a transient ischemic attack (TIA) or minor stroke. This group of patients is at high risk for having a recurrent stroke or TIA, and the investigators would like to investigate new ways of preventing potentially avoidable events. The treatment of sleep disorders immediately after a stroke or TIA may prove to be a novel method of avoiding future strokes and improving outcomes.

NCT ID: NCT01526824 Recruiting - Ischemic Stroke Clinical Trials

Lovaza's Effect on Clopidogrel in a Neuro Population

Start date: September 2011
Phase: Phase 0
Study type: Interventional

In patients who have suffered an ischemic stroke or TIA (mini-stroke), as well as in patients who are candidates for neuroendovascular stenting, it is standard of care to treat these patients with antiplatelet therapy, or "blood-thinners", the most common of which is clopidogrel (Plavix) with or without the addition of aspirin. A relatively common problem encountered with these patients is non-responsiveness to clopidogrel therapy. A prior study in cardiac patients showed that the addition of omega-3 polyunsaturated fatty acids (Lovaza, or "fish oil") can increase a patient's response to therapy with clopidogrel, but there have been no studies in neuro patients. In this study, patients will be divided into one of two groups: in the study arm, patients will receive clopidogrel +/- aspirin as well as Lovaza. In the control arm, patients will only receive clopidogrel +/- aspirin. Assays will be done to measure responsiveness to clopdiogrel on days 0, 12-24 hours after loading dose, day 3-5 if still inpatient, and at a follow-up visit 20-30 days after the start of the study. The investigators believe that this study will show an increase in platelet aggregation in patients receiving both clopidogrel and Lovaza.

NCT ID: NCT01520025 Terminated - Myocardial Ischemia Clinical Trials

Multi-modality Imaging of Ischemia With 18F-FDG PET and CTA

Start date: December 2011
Phase: Phase 4
Study type: Interventional

Coronary artery disease results in narrowing of the blood vessels supplying oxygenated blood to the heart muscle. Diagnosis in patients with symptoms of chest pain is now quickly done with CT coronary angiography. This x-ray test can show narrowed blood vessels but has limited ability to predict the severity of the narrowings in some cases. We have described a new approach using PET exercise 18F-FDG imaging as a method to image areas of heart muscle not getting enough blood during exercise stress. The 18F-FDG images are co-registered with the CT anatomy from the CTA to provide direct evidence of the consequences of the narrowing.

NCT ID: NCT01518842 Active, not recruiting - Ischemia Clinical Trials

Effect of Intravitreal Bone Marrow Stem Cells on Ischemic Retinopathy

RetinaCell
Start date: September 2011
Phase: N/A
Study type: Interventional

This study aims to evaluate the behavior of the intravitreal use of bone marrow derived stem cells in patients with ischemic retinopathy.

NCT ID: NCT01513824 Completed - Clinical trials for Ischemic Heart Disease

Stress and Ischemic Heart Disease. The Effect of Bio Feedback Guided Stress Management on Life Quality Including Signs of Depression and Stress

SongHeart
Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to examine if bio feedback guided stress management by daily measurement of pressure pain sensitivity followed by acupressure reduces signs of depression and number clinical stress signs and increases quality of life in patients with stable, ischemic heart disease

NCT ID: NCT01508910 Completed - Clinical trials for Refractory Angina Pectoris

Efficacy and Safety of Targeted Intramyocardial Delivery of Auto CD34+ Stem Cells for Improving Exercise Capacity in Subjects With Refractory Angina

RENEW
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the safety and efficacy of targeted intramyocardial delivery of Auto-CD34+ cells for increasing exercise time and amelioration of anginal symptoms in subjects with refractory angina and chronic myocardial ischemia.

NCT ID: NCT01502514 Withdrawn - Clinical trials for Ischemic Congestive Heart Failure

Safety and Efficacy of Adipose Derived Stem Cells for Congestive Heart Failure

Start date: May 2011
Phase: Phase 1
Study type: Interventional

The intent of this clinical study is to answer the questions: 1. Is the proposed treatment safe 2. Is treatment effective in improving the disease pathology of patients with Heart Disease as assessed by a series of measurements indicating improvement, stability, or degradation of a patient's cardiovascular function and exercise capacity?