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Cardiovascular Diseases clinical trials

View clinical trials related to Cardiovascular Diseases.

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NCT ID: NCT00927199 Completed - Clinical trials for Cardiovascular Disease

Efficacy of High-oleic Canola and Flaxseed Oils for Hypercholesterolemia and Cardiovascular Disease Risk Factors

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy of high-oleic canola oil and a high-oleic canola/flaxseed oil blend as compared to a typical Western diet on plasma lipids, fatty acid profiles, and risk factors associated with cardiovascular disease in hypercholesterolemic patients. Furthermore, the metabolism of dietary oleic acid and alpha-linolenic acid contained in high-oleic canola oil and flaxseed oil will be investigated.

NCT ID: NCT00926744 Active, not recruiting - Hypertension Clinical Trials

Nutrition and Exercise Intervention Study

NEXIS
Start date: April 2006
Phase: N/A
Study type: Interventional

The purpose of the present study was to clarify the effects of increase in physical activity on incidence and surrogate marker of cardiovascular diseases. The working hypothesis of the present study was that the physical activity to satisfy the Japanese guideline of Ministry of Health, Labour and Welfare is effective for the primary prevention of the lifestyle-related disease.

NCT ID: NCT00925483 Recruiting - Clinical trials for Cardiovascular Disease

Decreasing Dialysis Cardiovascular Risk: Daily Versus Longer Treatments

Start date: August 2004
Phase: N/A
Study type: Interventional

Given the known increased risk of heart disease in hemodialysis patients, this study aims to evaluate the change in both size and function of the heart by using cardiac magnetic resonance imaging (MRI) in patients undergoing either daily long (4 hours, 6 times weekly), daily short (2 hours 6 times weekly), or alternate day conventional (4 hours, 3 times weekly) and alternate day long (8 hours, 3 times weekly) dialysis for 6 months from randomization. The patients are randomly put in the groups based on predetermined randomization schedule and the cardiologist trained in cardiac MRI readings is blinded to the patient treatment schedule. Given that changes in heart function may be seen with cardiac imaging techniques within 6 months, the expectation is that groups on daily treatment may have better outcome for this parameter as changes in volume and blood pressure may also be affected in a positive way in patients on daily dialysis.

NCT ID: NCT00923039 Not yet recruiting - Clinical trials for Cardiovascular Disease

The Early Origins of Cardiovascular Disease

Start date: June 2009
Phase: N/A
Study type: Observational

Small body size at birth, slow weight gain during infancy and increase in body mass index after 2 years are independent risk factors for cardiovascular disease and the metabolic syndrome. There is a large gap in our understanding of how early growth affects the cardiovascular system. Possible mechanisms include alterations in body composition, in cardiac structure, in vascular function, in renal function and epigenetic processes. The Objective is to determine how size at birth and growth during infancy and childhood affect: body composition, cardiac structure and function, vascular and endothelial function, renal function, metabolic status and transcriptional and epigenetic characteristics.

NCT ID: NCT00921089 Completed - Clinical trials for Cardiovascular Diseases

Vascular Calcification, Inflammation and Coronary Flow Velocity in Hemodialysis Patients

Start date: April 2008
Phase: N/A
Study type: Observational

The aim of this cross-sectional study is to determine the correlation of coronary artery calcification as measured by electron-beam computerized tomography and coronary flow reserve measured by trans-thoracic Doppler echocardiography in hemodialysis patients. The investigators also assessed the carotid artery parameters by measuring intima media thickness that can accurately describe the process of arterial wall changes due to atherosclerosis. Possible association of coronary flow reserve with inflammation and arterial calcification in hemodialysis patients was also evaluated.

NCT ID: NCT00908297 Completed - Clinical trials for Cardiovascular Disease

Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients

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

The purpose of this study is to determine the safety and tolerability of the dietary supplement Coenzyme Q10 in hemodialysis patients.

NCT ID: NCT00908284 Completed - Clinical trials for Cardiovascular Diseases

Evaluating an Exercise Program to Reduce Cardiovascular Risk Factors in Children Infected With HIV

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

People infected with HIV are now living longer lives because of the use of highly active antiretroviral therapy (HAART). However, HAART medications have been shown to increase the risk of cardiovascular disease and metabolic dysfunction in adults. More research is needed on the effect of HAART in children. The purpose of this study is to assess cardiovascular risk factors in children infected with HIV who receive HAART medications and to determine the effectiveness of an exercise program on cardiovascular outcomes in these children.

NCT ID: NCT00907465 Completed - Clinical trials for Cardiovascular Disease

Sedentary Behavior in African Americans

SeBA
Start date: July 2007
Phase: N/A
Study type: Observational

The study is designed to develop methods for objectively measuring sedentary behavior, assess the association between objectively measured sedentary behavior and cardiovascular disease outcomes, and develop an intervention to reduce sedentary behavior, in African American adults.

NCT ID: NCT00904371 Completed - Hypertension Clinical Trials

Evaluation of the Effect of Telmisartan (Micardis® 80 mg/ MicardisPlus® 80/12.5 mg) on Blood Pressure and Cardiovascular Risk Factor Index in High Risk Hypertensive Patients

Start date: December 2009
Phase: N/A
Study type: Observational

The study is designed to evaluate the effect of treatment with Micardis/MicardisPlus on blood pressure and its ability to reduce different indicated cardiovascular risks. Further on, the study will evaluate the current antihypertensive treatment pattern in the daily practice among the patient population at increased cardiovascular risk.

NCT ID: NCT00901277 Completed - Clinical trials for Cardiovascular Disease

Supporting Post Myocardial Infarction (MI) Risk Modification Intervention Via Telemedicine Evaluation

SPRITE
Start date: June 2009
Phase: N/A
Study type: Interventional

The study is a three-arm design where up to 600 patients hospitalized post-MI are recruited from a large hospital and randomized to either the education group (control group) or one of the two intervention groups. Patients randomized to one of the intervention groups will receive a nurse-administered intervention plus the use of Microsoft's HealthVault web-based platform or solely the use of Microsoft's HealthVault web-based platform and web-based behavioral intervention, both of which includes a behavioral/medication management component. The 12 months effects of the intervention will be evaluated. For baseline and outcome assessments we will obtain BP, nonfasting LDL, and Hb A1c. Patients will also be surveyed about demographics and health behaviors during the baseline and 12 months. Study personnel serve as a liaison between subjects and their providers; however, all decisions related to clinical care are ultimately left up to the patient's provider. Subjects with serious adverse effects will be advised and assisted in seeking emergency medical care.