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Ischemia clinical trials

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NCT ID: NCT00224328 Terminated - Clinical trials for Peripheral Arterial Disease

Measurement of Tissue Oxygen Saturation in Chronic Critical Limb Ischemia

Start date: August 2005
Phase: Phase 2
Study type: Observational

Near-infrared spectroscopy can be used to determine the relative oxygen saturation in tissues up to 2cm below the skin. It has been investigated, with success, in cerebral, gastrointestinal, and muscle tissue, and shows promise in numerous indications involving tissue ischemia. In the current study, we propose to examine one hundred patients requiring either bypass or angioplasty due to chronic critical limb ischemia resulting from peripheral arterial disease. We intend to challenge patients before and after the intervention, using either an inflated blood pressure cuff or toe raises, to determine if oxygen saturation recovery time in the affected limb is correlated with symptom resolution (i.e. treatment success). Near-infrared spectroscopy will be performed using the ODISsey tissue oximeter developed by ViOptix, Inc. The proposed study will take approximately one year to complete enrolment, and has a follow-up period of 6 months post-intervention. Study Hypothesis: Knowledge of tissue oxygen saturation enhances clinical decision making in patients with chronic critical limb ischemia.

NCT ID: NCT00221182 Terminated - Clinical trials for Coronary Artery Disease

Stem Cell Study for Patients With Heart Disease

Start date: September 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if stem cell therapy with your own cells (autologous cells) delivered with a catheter to regions of the heart with poor blood flow will be safe and if it will relieve your chest pain, increase the blood flow, and/or improve the cardiac contractility (function) by regenerating blood vessels in your heart.

NCT ID: NCT00179010 Terminated - Ischemia Clinical Trials

AMP as a Better Delivery System of Adenosine

Start date: October 2003
Phase: Phase 1
Study type: Interventional

Adenosine and AMP are substances normally present in the body. Adenosine is also given for the treatment of some heart rhythm problems and may be used to reduce heart damage during heart attacks. The problem in using adenosine is that it is taken up by cells and, therefore, very little of the adenosine we give by vein or in the artery actually reaches the tissue. We propose to use AMP as a way to improve delivery of adenosine. AMP is inactive by itself, but is converted to adenosine in tissue. We hope that by giving AMP we will increase levels of adenosine in tissue. To see if this is true, we will give either adenosine or AMP into the forearm artery while we measure how much adenosine reaches the forearm tissue.

NCT ID: NCT00141011 Terminated - Stroke Clinical Trials

Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke

Start date: September 2005
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.

NCT ID: NCT00102128 Terminated - Clinical trials for Ischemic Heart Disease

Study to Examine the Safety and Effectiveness of Implanted Skeletal Muscle Cells (Cells Removed From the Thigh Muscle) Into Scarred Areas of Heart Muscle After Heart Attack.

Start date: November 2002
Phase: Phase 2
Study type: Interventional

Study to examine the safety and effectiveness of implanted skeletal muscle cells (cells removed from the thigh muscle) into scarred areas of heart muscle after heart attack.

NCT ID: NCT00060996 Terminated - Clinical trials for Critical Limb Ischemia

Study of Remodulin in Patients With Critical Limb Ischemia With No Planned Revascularization Procedures

Start date: February 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess and compare the safety of continuous and daily subcutaneous Remodulin therapy in patients with critical limb ischemia (CLI) with no planned vascular interventional procedures; and to determine the effect of Remodulin on wound healing and treadmill walk distance.

NCT ID: NCT00060450 Terminated - Clinical trials for Ischemia-Reperfusion Injury

Inhaled Nitric Oxide in Prevention/Treatment of Ischemia-Reperfusion Lung Injury Related to Lung Transplantation

Start date: August 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effects of inhaled nitric oxide on both short-term physiology as well as on the development of ischemia-reperfusion lung injury (IRLI) in the immediate post transplant period. The specific hypothesis is that inhaled NO post lung transplantation will improve gas exchange/hemodynamic and thus reduce the development of post transplant IRLI.