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Ischemia clinical trials

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NCT ID: NCT01866189 Withdrawn - Ischemic Stroke Clinical Trials

Identification of Hypoxic Brain Tissues by F-MISO PET in Acute Ischemic Stroke

STROKE F-MISO
Start date: September 2016
Phase: N/A
Study type: Interventional

This study is a French multicenter prospective study including 5 stroke units with available MRI and F-MISO PET for patients with acute ischemic stroke. Background and Purpose: 18F-Fluoromisonidazole (FMISO) PET has been used to identify hypoxic tissues in animals and stroke patients. While MRI has become the gold standard acute stroke imaging, no published study has compared FMISO PET and MRI. The aim of this prospective study is to identify hypoxic tissues in 40 patients with acute ischemic stroke with F-MISO PET and to compare the location and the outcome of these hypoxic cells with MRI datas (weighted diffusion and FLAIR) and to clinical outcome.

NCT ID: NCT01849887 Withdrawn - Ischemic Stroke Clinical Trials

Safety of Escalating Doses of Intravenous Bone Marrow-Derived Mesenchymal Stem Cells in Patients With a New Ischemic Stroke

Start date: January 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Stroke is a major cause of adult disability. Currently approved reperfusion therapies are provided to only a small percentage of patients in the U.S. New therapies are needed that improve outcome and that can be accessed by a majority of patients. Animal studies suggest that bone marrow-derived mesenchymal stem cells, administered intravenously days after a stroke, safely improve long-term behavioral outcome. A large human experience suggests the safety of allogeneic bone marrow-derived mesenchymal stem cells. The current study aims to assess the safety of this therapy in patients with recent ischemic stroke.

NCT ID: NCT01825239 Withdrawn - Cardiomyopathy Clinical Trials

Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy

Start date: April 2014
Phase: N/A
Study type: Interventional

Presently, the left ventricular lead is placed in a similar position for all patients. It is not known whether placing this lead in different positions in the heart will make the heart pump better. In this study, the investigator will collect measurements of the heart's electrical activity during an Electrophysiology Study (EP study or EPS). The hope is that these measurements will provide the know how to develop an individualized left ventricular lead placement "prescription" for patients referred for left ventricular lead pacing.

NCT ID: NCT01728649 Withdrawn - Ischemic Stroke Clinical Trials

Reperfusion With Cooling in Cerebral Acute Ischemia II

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

The purpose of this study is to determine whether reducing a patients body temperature (mild hypothermia of 33 degrees Centigrade) will significantly reduce the risk of brain injury (notably reperfusion injury and hemorrhagic conversion) in patients that have suffered a significant interruption of blood flow to an area of brain (occlusion of large proximal cerebral artery) and have undergone successful removal of that interruption (revascularization).This will be achieved by comparing patients that have undergone hypothermia to those that have not.

NCT ID: NCT01628055 Withdrawn - Ischemic Stroke Clinical Trials

IVIG in Acute Ischemic Stroke: A Pilot Study

IVIG/AIS
Start date: March 2013
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the ability of IVIG to affect the rate of progression of brain ischemia, as evidenced by neuroimaging. The results of an ongoing epidemiological study indicate that patients with primary immunodeficiency (PID) on IVIG replacement therapy have an overall prevalence of stroke that is 5 times less than in the general population. Even more striking is the absence of stroke in IVIG-treated PID patients over 65, while in the same general population age group the stroke prevalence goes up to 8.1%. This suggests that the degree of stroke protection correlates with the length of IVIG treatment, since older PID patients have been treated with IVIG significantly longer than younger ones.

NCT ID: NCT01614379 Withdrawn - Clinical trials for Diabetes Mellitus, Type 1

Non-enhanced Magnetic Resonance Angiography of Diabetic Ischemic Lower Limbs

Start date: June 2012
Phase: N/A
Study type: Observational

Diabetic foot ulcers often progresses after many years of diabetes where the patients system is so damaged that normal heeling of ulcers cannot happen. The physician at the clinic examines the foot, measuring its circulation and sensitivity. The measures are the blood pressure in comparison between foot and upper arm and oxygen level in the foot. The measurements have a direct connection to the blood circulation, but it doesn't visualize the blood circulation. Development of MR methods without the use of contrast agents have become so good that images of the blood veins can be used in treatment. This means that the MR images provide important information about the patient vessel wall stiffness and blood circulation without the use of the damaging substances. Hence the physician can perform the MR examination and in comparison with the test performed at the clinic he can make an improved and without risk diagnose. Using MR at a lot earlier stage in the treatment is expected to reduce the number of amputations. This is not only an economic advantage, but also an improvement of the patient quality of life. The objective of the study is to investigate type 1 diabetics oxygen level, vessel wall stiffness, blood circulation, tissue contribution and blood pressure in the foot with the use of conventional measurements in their treatment and with the added use of MR methods. This will provide the physician with valuable information of the patient illness and is expected to play an important role in the prevention of diabetic foot ulcers. We expect that MR research leads to a much improved prevention and treatment of aggressive and destructive diabetic foot ulcers. This will increase the general quality of life and reduce the large number of amputations performed every year.

NCT ID: NCT01607671 Withdrawn - Clinical trials for Ischemic Optic Neuropathy

Treatment Study for Ischemic Optic Neuropathy With Opthalmic Timolol Maleate 0.5%

Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the feasibility of rapid evaluation and administration of ophthalmic Timolol maleate in the treatment of non-arteritic anterior ischemic optic neuropathy. Secondary goals are to evaluate if such treatment reduces the progression or improves recovery of patients who are randomly assigned to treatment versus standard of care.

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?

NCT ID: NCT01496209 Withdrawn - Clinical trials for Ischemic Cardiomyopathy

REgenerative CardiOsphere iNjection to STRengthen dysfUnCTional Hearts

RECONSTRUCT
Start date: July 2015
Phase: Phase 1
Study type: Interventional

A double blinded and placebo-controlled, dose escalation, single-center safety and preliminary efficacy study of cardiospheres delivered via NOGA MYOSTAR injection catheter in subjects with chronic ischemic cardiomyopathy. The objective is to achieve and document myocardial regeneration in patients with chronic scar.

NCT ID: NCT01357499 Withdrawn - Clinical trials for Ischemic Heart Disease

Lower Leg Remote Ischemic Preconditioning in Elective Percutaneous Coronary Intervention (PCI)

REMOTE
Start date: December 2010
Phase: Phase 0
Study type: Observational

The purpose of this study is to investigate if remote ischemic preconditioning by combining limb ischaemia with electric muscle stimulation of the ischemic muscle provokes better results in preconditioning the human heart than limb ischaemia alone does.