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Arteriosclerosis clinical trials

View clinical trials related to Arteriosclerosis.

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NCT ID: NCT00174902 Active, not recruiting - Clinical trials for Stress, Psychological

The Effect of Beta-Blockers and Aspirin on Hemostasis and Endothelial Function After Acute Mental Stress

Start date: October 2003
Phase: Phase 1/Phase 2
Study type: Interventional

This randomized double-blinded controlled trial uses a factorial design to investigate whether application of beta-blockers (inderal 80 mg) or aspirin (100 mg) or a combination thereof has an effect on the activation of the hemostatic system, the platelets and the endothelium in response to acute mental stress. Specifically we test the hypothesis that inderal attenuates the activation of the hemostatic system as compared to placebo. The second hypothesis is that aspirin attenuates the activation of platelets as compared to placebo. Subjects will be randomly allocated to either of the four following study arms: placebo - inderal - aspirin - inderal plus aspirin. Subjects will receive the study medication for five days prior to the mental stress. The acute mental stress consists of a public speaking session of 10 min duration immediately followed by a mental arithmetic test of 5 min duration. Blood will be collected prior to the stress, immediately thereafter, at 45 min at at 1 hour and 45 min.

NCT ID: NCT00172536 Completed - Clinical trials for Coronary Arteriosclerosis

Effects of Exercise Training on Left Ventricular Function in Type 2 Diabetic Patients Post Coronary Artery Bypass Graft

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

The purpose of this study is to investigate the changes of cardiorespiratory fitness and left ventricular function in type 2 diabetes after uncomplicated coronary artery bypass graft (CABG) surgery. We hypothesize that exercise capacity, left ventricular diastolic function, and biochemical data improves after 12-wk exercise training in patients with type 2 diabetes underwent CABG.

NCT ID: NCT00163202 Completed - Clinical trials for Hypercholesterolemia

Comparative Atorvastatin Pleiotropic Effects

CAP
Start date: June 2002
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to evaluate the efficacy of atorvastatin 80 mg daily as compared to atorvastatin 10 mg daily in reducing C-reactive protein levels over a 26-week treatment period in subjects with documented coronary artery disease.

NCT ID: NCT00161070 Completed - Clinical trials for Transient Ischemic Attack

ESPRIT: European/Australasian Stroke Prevention in Reversible Ischaemia Trial

Start date: July 1997
Phase: Phase 4
Study type: Interventional

The objective of ESPRIT was to compare the efficacy and safety of mild anticoagulation or a combination treatment of aspirin and dipyridamole with the efficacy and safety of treatment with aspirin alone after cerebral ischemia of arterial origin.

NCT ID: NCT00159991 Active, not recruiting - Clinical trials for Ischemic Heart Disease

Copenhagen Arterial Revascularization Randomized Patency and Outcome Trial

CARRPO
Start date: February 2002
Phase: Phase 3
Study type: Interventional

There is a remarkable lack of randomized trials concerning the potential benefit of using arterial conduits for coronary bypass surgery. This is the purpose of the present trial. Exclusive use of arterial conduits might result in improved conduit viability, reduced risk of recurrent angina, myocardial infarction and other cardiac events, reduced need for antianginal medication, improved functional status and possibly improved long term survival. The patients will be followed for ten years after surgery.

NCT ID: NCT00159926 Terminated - Clinical trials for Coronary Arteriosclerosis

Cleansing of Suction Blood in Cardiac Surgery for Reduced Inflammatory Response

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

Cardiac surgery using heart and lung machine produces an inflammatory reaction in the body. This leads in few percent of cases to heart, lung, and kidney disturbances that potentially causes death. White blood cells in contact with the heart and lung machine and external surfaces release mediators partly responsible for this. Blood collected by the suction and the blood remaining in the heart and lung machine after its use, can be cleaned by a cell saver before reinfusion, and this might reduce the inflammatory response.

NCT ID: NCT00155012 Recruiting - Clinical trials for Coronary Arteriosclerosis

Clinical Application of MDCT in Coronary Artery Disease

Start date: August 2004
Phase: Phase 3
Study type: Observational

1) Establish normal value for coronary calcium scoring in Taiwan. 2) Find out the relationship of coronary calcium deposition and coronary artery stenosis. Propose a clinical management guideline based on coronary calcium score. 3) Evaluate sensitivity/specificity of coronary CT angiography and the influence of coronary calcium score on coronary CT angiography. 4) Evaluate the clinical application of myocardial enhancement measurement.

NCT ID: NCT00154180 Active, not recruiting - Menopause Clinical Trials

Kronos Early Estrogen Prevention Study (KEEPS)

Start date: September 2005
Phase: Phase 4
Study type: Interventional

The study will examine the effects of estrogen and progesterone on the development of atherosclerosis in menopausal women when hormone treatment is initiated within 3 years of the menopausal transition.

NCT ID: NCT00145262 Recruiting - Clinical trials for Arteriosclerosis Obliterans

TACT-NAGOYA: Therapeutic Angiogenesis Using Cell Transplantation

Start date: August 2003
Phase: Phase 2
Study type: Observational

Clinical studies have established that implantation of bone marrow mononuclear cells (BM-MNCs) or peripheral blood mononuclear cells (PB-MNCs) into ischaemic limbs increases collateral vessel formation. We, the investigators at Nagoya University, further investigated the efficacy and safety of autologous implantation of BM-MNCs or PB-MNCs in patients with severe ischaemic limbs who have no other alternative therapeutic options. We also examined a potential limiting factor which reduced the efficacy of therapeutic angiogenesis using cell transplantation (TACT).

NCT ID: NCT00139399 Completed - Clinical trials for Coronary Arteriosclerosis

Radial Artery Versus Saphenous Vein Patency (RSVP) Study

RSVP
Start date: May 1998
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the radial artery (artery in the arm) or saphenous vein (vein in the leg), when used as bypass grafts for coronary artery bypass surgery, have a greater patency rate (degree of opening)at 5 years after surgery.