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Syndrome clinical trials

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NCT ID: NCT00728013 Recruiting - Clinical trials for Acute Coronary Syndrome

China Intensive Lipid Lowering With Statins in Acute Coronary Syndrome

CHILLAS
Start date: December 2006
Phase: N/A
Study type: Interventional

In summary, the CHILLAS study will be the first multicenter study performed in a Chinese population using a patient-level analysis to compare the effects and safety of intensive statin therapy with that of moderate statin therapy. Therefore, it will determine whether "lower is better", that is, whether LDL cholesterol lowering to a level of approximately 100mg/dl provides a benefit inferior to that of LDL cholesterol lowering to a much lower level; examine the role of inflammatory markers in predicting cardiac events and response to statin therapy; and evaluate the effects of statin therapy on regression of coronary atherosclerosis using IVUS.

NCT ID: NCT00727779 Completed - Metabolic Syndrome Clinical Trials

Mechanisms by Which Strength Training Ameliorates the Metabolic Syndrome

Start date: January 2008
Phase: N/A
Study type: Interventional

Prevention and treatment strategies for diabetes use exercise as the cornerstone. Even though endurance training and strength training both improve insulin resistance, strength training may be better suited for persons at risk for type 2 diabetes. We will expand our pilot studies of muscle adaptation induced by resistance exercise training to determine the biochemical mechanisms that will cause people with the Metabolic Syndrome to secure major benefit from intense strength training.

NCT ID: NCT00726830 Terminated - Pain Clinical Trials

Methadone, Morphine, or Oxycodone in Treating Pain in Patients With Cancer

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

RATIONALE: Methadone, morphine, or oxycodone may help relieve pain caused by cancer. It is not yet known whether methadone is more effective than morphine or oxycodone in treating pain in patients with cancer. PURPOSE: This randomized clinical trial is studying methadone to see how well it works compared with morphine or oxycodone in treating pain in patients with cancer.

NCT ID: NCT00725829 Unknown status - Clinical trials for Acute Coronary Syndrome

Hypolipemic Treatment in Acute Coronary Syndrome (ACS): Antithrombotic Effects

Start date: June 2008
Phase: N/A
Study type: Interventional

The aim of the current study is to evaluate whether treatment with high doses of simvastatin can reduce coagulation activation in patients with acute coronary syndromes and if ezetimibe in conjunction with simvastatin may affect blood clotting in a similar manner. The investigators hypotheses are as follows: 1. Intensive lipid lowering treatment with simvastatin (40 mg/day) and simvastatin (40 mg/day) combined with ezetimibe (10 mg/day) initiated after acute coronary syndrome leads to attenuation of blood coagulation including reduced thrombin generation, thrombin-mediated coagulant reactions, and improved structure of plasma clots. 2. Anticoagulant effects of simvastatin are weaker than those observed during administration of simvastatin and ezetimibe.

NCT ID: NCT00725062 Terminated - Lymphoma Clinical Trials

Donor T Cells in Treating Patients With High-Risk Hematologic Cancer Undergoing Donor Peripheral Blood Stem Cell Transplant

Start date: June 2008
Phase: Phase 1
Study type: Interventional

RATIONALE: A donor peripheral stem cell transplant helps stop the growth of cancer cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Once the donated stem cells begin working, the patient's immune system may see the remaining cancer cells as not belonging in the patient's body and destroy them. Giving an infusion of donor T cells may helps stop the patient's immune system from rejecting the donor's stem cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of donor T cells in treating patients with high-risk hematologic cancer who are undergoing donor peripheral blood stem cell transplant. Note: Only Phase I portion of study was performed. Due to slow accrual, study was closed before Phase II portion of study.

NCT ID: NCT00724126 Completed - Clinical trials for Non-Constipation Irritable Bowel Syndrome

Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)

TARGET 2
Start date: July 2008
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of a 14-day course of rifaximin given 3 times a day vs. placebo in providing adequate relief of IBS symptoms.

NCT ID: NCT00723801 Completed - Marfan Syndrome Clinical Trials

Effects of Losartan Versus Atenolol on Aortic and Cardiac Muscle Stiffness in Adults With Marfan Syndrome

Start date: October 2007
Phase: Phase 3
Study type: Interventional

Marfan syndrome is an inherited connective tissue disorder with morbidity and mortality from aortic dilation and dissection. The degree of aortic dilation and response to beta-blockade (standard of care) vary in adults with Marfan syndrome. However, aortic stiffness is often present, and can be a predictor of aortic dilation and cardiovascular complications. In addition, adults with Marfan syndrome develop left ventricular diastolic dysfunction, which can progress to heart failure. Aortic stiffness and diastolic dysfunction are important and logical therapeutic targets in adults with Marfan syndrome. TGF-beta mediates disease pathogenesis in Marfan syndrome and contributes to aortic stiffness. The angiotensin receptor blocker, losartan, inhibits TGF-beta activity and reverses aortic wall pathology in a Marfan mouse model. Losartan also decreases aortic stiffness and improves diastolic function in hypertension, renal disease and hypertrophic cardiomyopathy. This trial is a randomized, double-blind trial of 50 adults with Marfan syndrome, treated with 6 months of atenolol vs. losartan. Arterial tonometry for aortic stiffness and echocardiography for diastolic function will be performed at the beginning and end of treatment. A blood draw for serum markers of extracellular matrix turnover and inflammation will also be performed at 0 and 6 months. We plan to determine whether losartan decreases aortic stiffness and left ventricular diastolic dysfunction significantly more than atenolol.

NCT ID: NCT00723112 Completed - Clinical trials for Myelodysplastic Syndrome

The Role of Erythropoietin in Myelodysplastic Syndrome

Start date: February 2007
Phase: N/A
Study type: Observational

The purpose of the study is to elucidate the causative molecular events responsible for the abnormal erythropoiesis in MDS.

NCT ID: NCT00721656 Completed - Dry Eye Syndromes Clinical Trials

Phase 2 Study of KLS-0611 in Patients With Dry Eye Syndromes

Start date: n/a
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of KLS-0611 compared to placebo in patients with dry eye syndromes.

NCT ID: NCT00721214 Completed - Clinical trials for Myelodysplastic Syndrome

5-Azacytidine Prior to Allogeneic Stem Cell Transplant in High Risk Myelodysplastic Syndrome

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the feasibility and efficacy of using the demethylating agent 5-Azacytidine prior to allogeneic stem cell transplantation in patients with high risk myelodysplastic syndrome (MDS).