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Ischemic Heart Disease clinical trials

View clinical trials related to Ischemic Heart Disease.

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NCT ID: NCT02339857 Completed - Atherosclerosis Clinical Trials

The Long-term Results of the No-touch Vein Graft to the Left Anterior Descending Artery.

Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of this study was to investigate whether the no-touch saphenous vein grafts that were used in coronary artery bypass surgery between 2003-2008 had a patency rate comparable to the left internal thoracic artery when the vein grafts were anatomised to the left anterior descending artery.

NCT ID: NCT02292888 Not yet recruiting - Clinical trials for Ischemic Heart Disease

Can Changes in Velocity Time Integral Serve as a Sensitive Indicator for Monitoring Changes in Stroke Volume ?

Start date: December 2014
Phase: Phase 0
Study type: Interventional

Hypothesis: A validated technique to measure cardiac output (CO) using echocardiography is to calculate stroke volume from the product of LVOT area and LVOT VTI and multiplying the product with heart rate ( CO = SV x H/R; SV = LVOT area x LVOT VTI ). The LVOT diameter for an individual is more or less a constant measurement. Therefore using the formula mentioned above (SV = LVOT area x LVOT VTI), if the LVOT area is constant, then SV should be proportional to the VTI. This means if a PLR manoeuvre or fluid bolus helps to achieve a rise in SV, then it should be reflected in an increase in VTI as well. If this assumption is true, then an increase in the value of VTI from baseline after fluid challenge (10-15%), should identify a volume responsive patient.

NCT ID: NCT02230098 Completed - Clinical trials for Ischemic Heart Disease

Effects of Remote Ischemic Conditioning on Myocardial Perfusion in Humans

CONDI-PET
Start date: August 2013
Phase: Phase 3
Study type: Interventional

Cardiovascular disease is the second leading cause of death in Denmark, and ischemic heart disease accounts for the bulk of it. The purpose of this study is to clarify whether a mechanical method of remote ischemic conditioning in the form of short-term obstruction of the blood supply to the arm, can improve the heart's blood supply in patients with ischemic heart disease. This will be attempted through experiments on patients with ischemic heart disease and experimental animal studies with simulated cardiovascular disease. This study will help to clarify whether remote ischemic preconditioning can be used to treat patients with ischemic heart disease.

NCT ID: NCT02202967 Completed - Atrial Fibrillation Clinical Trials

Misoprostol for Small Bowel Ulcers and Obscure Bleeding Due to Aspirin or Nonsteroidal Antiinflammatory Drugs

MASTERS
Start date: January 7, 2016
Phase: Phase 3
Study type: Interventional

Anti-inflammatory tablets (non-steroidal anti-inflammatory drugs) continue to be used commonly worldwide to relieve pain caused by arthritis. Likewise, aspirin is used by many patients in order to prevent blood clots. Despite their desired benefits, these medicines can cause internal bleeding from the digestive system. The source of this bleeding can be obvious (overt), or obscure and thought to come from the small intestine. Obscure bleeding can show as anemia due to lack of iron in the blood. Small intestine ulcers are now easily diagnosed using an endoscope the size of a big pill (video capsule endoscopy). Small bowel ulcers are not related to stomach acid and therefore do not heal using remedies usually taken to stop acid formation. A different drug, misoprostol, consists of a chemical (prostaglandin) that is usually lacking in patients using aspirin or anti-inflammatory drugs. Misoprostol is licenced to heal stomach and duodenal ulcers in patients using these drugs. Our hypothesis is that misoprostol might be effective in healing small bowel ulcers as suggested by pilot studies; however, such works only included small numbers of patients, did not include control groups and both patients and investigators knew the nature of the tablets used. To test this hypothesis, we propose to compare misoprostol to a dummy tablet. The numbers of subjects to be studied have been calculated using established statistical methods

NCT ID: NCT02162082 Completed - Clinical trials for Coronary Artery Disease

Coronary and Structural Interventions Ulm - Coronary Chronic Total Occlusions

CSI-Ulm-CTO
Start date: June 2014
Phase: N/A
Study type: Interventional

To evaluate the long-term results after recanalization of coronary chronic total occlusions.

NCT ID: NCT02162056 Completed - Clinical trials for Coronary Artery Disease

Coronary and Structural Interventions Ulm - Bioresorbable Vascular Scaffold

CSI-Ulm-BVS
Start date: November 2013
Phase: N/A
Study type: Interventional

To evaluate the safety, performance and efficacy of the bioresorbable vascular scaffold (BVS) system in patients with coronary artery disease

NCT ID: NCT02159235 Completed - Clinical trials for Coronary Artery Disease

Heavy Metals, Angiogenesis Factors and Osteopontin in Coronary Artery Disease (CAD)

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

The present study aims is to investigate: 1. whether patients suffering from acute resp. chronic ischemic heart disease show higher levels for cadmium (Cd), lead (Pb) and mercury (Hg) than local and international reference levels suggest; 2. the correlation between severity of coronary artery disease and angiogenic and angiostatic factors (endostatin-ES, angiostatin-AS, VEGF-vascular endothelial growth factor, osteopontin-OPN) The patient population consists of about 270 female and male patients suffering either acute or chronic ischemic heart disease (AIHD:ICD-10 I21; CIHD: ICD-10 I25). 3. whether patients suffering CAD and valve calcification (mitral annulus, aortic valve) show higher levels of endostatin, angiostatin, osteopontin and VEGF compared to patients with CAD but without valve (annulus) calcification The measurement of cadmium (urine), lead, mercury, zinc, endostatin, angiostatin, VEGF (serum) and osteopontin (plasma) in patients with angiographically verified coronary artery disease are in the fore. Furthermore, basic laboratory diagnostics as well as data from coronary angiography and echocardiography will be collected. Additionally, the investigators will inquire heavy metal exposition during life by an interview. Recruitment will be done during the in-patient stay at the General Hospital of Vienna, Medical University of Vienna.

NCT ID: NCT02133287 Active, not recruiting - Clinical trials for Acute Coronary Syndrome

To Evaluate The Safety and Efficacy of 'AVI' Stent Comparing With Firebird2® For Treating Coronary Revascularization

Start date: August 2013
Phase: N/A
Study type: Interventional

To evaluate The Safety and Efficacy of 'AVI' Stent Comparing with Firebird2® For Treating Coronary Revascularization.

NCT ID: NCT02131142 Active, not recruiting - Clinical trials for Ischemic Heart Disease

BioFreedom US IDE Feasibility Trial

Start date: August 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to collect additional safety and effectiveness data for on the Biosensors BioFreedomâ„¢ BA9 Drug Coated Coronary Stent in patients with native, de novo coronary artery disease.

NCT ID: NCT02117843 Recruiting - Clinical trials for Acute Coronary Syndrome

The Safety and Efficacy of 'AVI' Stent for Treating Coronary Revascularization

Start date: July 2013
Phase: N/A
Study type: Interventional

The study is a Prospective, Multi-center, Single Armed Registry to Evaluate The Safety and Efficacy of 'AVI' Stent for Treating Coronary Revascularization.