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Endothelial Dysfunction clinical trials

View clinical trials related to Endothelial Dysfunction.

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NCT ID: NCT00385151 Completed - Clinical trials for Endothelial Dysfunction

To Compare the Ischemic Pre-conditioning and Post-conditioning on Reperfusion Injury in Humans.

Start date: May 2006
Phase: N/A
Study type: Observational

Reperfusion Injury occurs by the sudden blood flow to the injured and ischemic myocardium during restoration of blood flow either by Mechanical revascularization or thrombolysis. A phenomenon known as Pre-conditioning has been identified to limit the the extent and severity of reperfusion injury but it is very difficult to apply it in patient care setting as timing of acute cardiac or neurologic ischemic event is difficult to reliably predict. Postconditioning or ischemic postconditioning is well known to attenuate the reperfusion injury. There is enough data that shows the benefit of post conditioning in reducing the reperfusion injury in animals. However postconditioning in humans has not been investigated. We hypothesize that Post conditioning will attenuate the reperfusion injury and will be comparable to the effect of preconditioning in humans.

NCT ID: NCT00384683 Completed - Clinical trials for Endothelial Dysfunction

Endothelial Dysfunction As A Predictor Of Perioperative Outcome

Start date: March 2006
Phase:
Study type: Observational

The goal of this clinical research study is to learn whether the inability of certain blood vessel cells (endothelial cells) to function properly may help researchers to predict who is at risk for complications after surgery and whether this dysfunction contributes to complications after surgery. This study will use a blood test to quantify the number of cells that are destined to become endothelial cells.

NCT ID: NCT00376246 Completed - Clinical trials for Endothelial Dysfunction

Effect of Ezetimibe on Flow-mediated Brachial Artery Reactivity in Healthy Subjects

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The objective of this study is to show that Ezetimibe will improve endothelial function following high cholesterol meals in healthy subjects by decreasing absorption of cholesterol and thus affecting concentration and composition of remnant-like particles.

NCT ID: NCT00358306 Completed - Clinical trials for Endothelial Dysfunction

The Role of Endothelium Dysfunction in Progression of CKD (Chronic Kidney Disease) After AKI (Acute Kidney Injury)

Start date: April 2008
Phase:
Study type: Observational

To understand how AKI (Acute Kidney Injury) leads to chronic kidney disease so therapies can be found to alter the progression of events thereby significantly impacting the long-term outcomes of children who develop AKI.

NCT ID: NCT00271492 Completed - Clinical trials for Endothelial Dysfunction

Correlation of Endothelial Function and Early Coronary Artery Disease in Humans

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

Qualifying patients who are scheduled for angiogram with endothelial function testing are approached to participate in this protocol (consent form reviewed with patient). Those who are willing to participate will have additional measurements taken during their angiogram as part of this protocol. Patients who are diagnosed with Endothelial Dysfunction as a result of a clinically indicated angiogram will be eligible to participate in a 6 month medication trial (Atrasentan vs. placebo - randomized, blinded trial). Patients are monitored closely during the 6 month trial via phone calls and blood testing for assessment. At the end of the 6 months they return to Mayo for a repeat angiogram to assess endothelial function for any changes or improvements.

NCT ID: NCT00214825 Completed - Diabetes Mellitus Clinical Trials

Aldosterone and Vascular Disease in Diabetes Mellitus

Start date: August 2003
Phase: N/A
Study type: Interventional

Specific aims for this proposal are to determine in patients with diabetes mellitus the effects of an aldosterone receptor antagonist on: 1. Coronary microvascular function assessed by MRI perfusion reserve, 2. Endothelial dysfunction assessed by brachial artery reactivity studies, and 3. Inflammation assessed by blood measurements of c-reactive protein (CRP), monocyte chemoattractant protein-1 (MCP-1), and plasminogen activator inhibitor-1 (PAI-1).