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Cardiovascular Diseases clinical trials

View clinical trials related to Cardiovascular Diseases.

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NCT ID: NCT01355406 Completed - Clinical trials for Cardiovascular Diseases

Evaluation of Safety and Efficacy of the FlexStent® Femoropopliteal Self-Expanding Stent System

OPEN
Start date: September 16, 2011
Phase: N/A
Study type: Interventional

This is a clinical study of a new self-expanding stent (FlexStent®) designed specifically to cope with the extreme demands of the superficial femoral artery (SFA)/proximal popliteal artery. The arteries are often abbreviated as femoropopliteal. The intent of this study is to demonstrate that the FlexStent® Femoropopliteal Self-Expanding Stent System is safe and effective for the treatment of patients with peripheral arterial disease. Specifically, the FlexStent® shall meet or exceed the proposed safety and efficacy performance goals established for Femoropopliteal bare nitinol stents in patients with symptomatic peripheral arterial disease.

NCT ID: NCT01353066 Not yet recruiting - Clinical trials for Atherosclerotic Cardiovascular Disease

Gastric Bypass Versus Best Medical Treatment on Progression of Carotid-intima Media Thickness in Type 2 Diabetes Mellitus (T2DM)

EURDSS
Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Type 2 Diabetes Mellitus (T2DM) is associated with an increased burden for cardiovascular disease (CVD). Multifactorial interventions are necessary to reduce the CV risk in T2DM. Bariatric surgery appears to be an alternative for the multifactorial intervention in T2DM associated with obesity. Data have shown, that clinical trial aiming at the control of CVRF in T2DM may not translate in the reduction of CV events. Hypothesis: Intensive medical treatment (IMM) including Roux-en-Y Gastric Bypass (RYGBP) could be superior in the control of the progression of subclinical atherosclerotic disease, as evaluated by carotid ultrasound, in subjects with T2DM and a BMI between 30.0 and 34.9 kg/m2.The primary aim of the study is To compare the effects of intensive medical treatment (IMM) including Roux-en-Y Gastric Bypass (RYGBP) and IMM alone on the progression of the carotid intima media thickness (CIMT) at 24 months after entry into the trial relative to baseline.Methodology: Two-year Randomized Clinical Trial, including 240 patients

NCT ID: NCT01353001 Completed - Obesity Clinical Trials

Effect of Weight Loss on Cardiovascular Disease Risk Factors in Obese Women

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effect of weight loss and exercise on cardiovascular disease risk factors, specifically inflammation as measured by C-Reactive Protein and cardiac structure and function as measured by cardiac MRI, in Class II and III obese women during a 12 week training intervention.

NCT ID: NCT01351012 Completed - Metabolic Syndrome Clinical Trials

Canola Oil Multicentre Intervention Trial

COMIT
Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of the study is to examine how the consumption of different dietary oil varieties affects a broad range of metabolic responses that are important in the development of cardiovascular diseases. This study will examine the relationship between dietary oil consumption and arterial function, blood fat content, and blood markers of cardiovascular disease risk. Additionally, the efficiency of the body in converting fat from dietary oils into other specific fat compounds with know health benefits will be examined. Also, the correlation between psychosocial parameters and vascular function will be studied.

NCT ID: NCT01346189 Completed - Clinical trials for Cardiovascular Disease

A Trial of Behavioral Economic Interventions to Reduce Cardiovascular Disease (CVD) Risk

Start date: September 2011
Phase: N/A
Study type: Interventional

Using a 4-arm, cluster-randomized controlled trial, the investigators will test the effectiveness of different behavioral economic interventions in increasing statin use and reducing LDL cholesterol among patients with poor cholesterol control who are at very high risk for CVD. The investigators will test these approaches among primary care physicians and their patients at very high risk of CVD at Geisinger Health System and University of Pennsylvania outpatient clinics.

NCT ID: NCT01346072 Completed - Heart Failure Clinical Trials

Pilot Study of Using Copeptin to Predict Response to Tolvaptan

Start date: April 2011
Phase: Phase 4
Study type: Interventional

This study will investigate the association between levels of the peptide copeptin and response to tolvaptan, a drug that blocks the action of the water retaining hormone vasopressin.

NCT ID: NCT01343810 Completed - Clinical trials for Cardiovascular Diseases

Stress Reduction Training to Improve Sleep Quality, Stress Physiology & Cardiovascular Disease (CVD) Risk Markers

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

The goal of this study is to better understand the potential value of reducing stress to ameliorate a cluster of biological and behavioral factors implicated in cardiovascular disease (CVD) risk. These factors include psychological distress, poor sleep quality, and exaggerated physiological responses to emotional stress. Results will be used to develop an innovative brief intervention to reduce risk for CVD by improving sleep quality, ameliorating psychological distress, and attenuating stress physiology.

NCT ID: NCT01343667 Completed - Clinical trials for Cardiovascular Diseases

GORE Flow Reversal System and GORE Embolic Filter Extension Study

FREEDOM
Start date: April 2011
Phase: N/A
Study type: Interventional

The objective of this study is to provide an ongoing evaluation of clinical outcomes associated with the GORE Flow Reversal System and the GORE Embolic Filter when used for embolic protection during carotid artery stenting.

NCT ID: NCT01343342 Active, not recruiting - Clinical trials for Cardiovascular Disease

Genes, Omega-3 Fatty Acids and Cardiovascular Disease Risk Factors

FAS
Start date: October 2009
Phase: N/A
Study type: Interventional

The main purpose of this study is to examine whether n-3 PUFA-induced changes in metabolic risk factors are influenced by genetic variations within genes acting as fatty acids sensors.

NCT ID: NCT01339611 Recruiting - Atrial Fibrillation Clinical Trials

Education Program for Patients Receiving Oral Anticoagulation

Start date: May 2011
Phase: N/A
Study type: Interventional

The aim of the study is to test if patients under oral anticoagulation therapy who are going to participate in the education program will have better Health-related quality of life, higher rate in pharmacological treatment adherence and better self efficacy to manage the treatment.