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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT01386021 Completed - Clinical trials for Coronary Artery Disease

Saphenous Vein Allografts for Coronary Bypass

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

The primary objective of this observational study is to evaluate the function (patency) of cryopreserved saphenous vein allografts used as coronary artery bypass grafts (CABG) for patients with occlusive coronary artery disease.

NCT ID: NCT01385319 Active, not recruiting - Clinical trials for Coronary Artery Disease

Zotarolimus-eluting Endeavor Sprint Stent in Uncertain DES Candidates (ZEUS) Study

ZEUS
Start date: June 2011
Phase: Phase 3
Study type: Interventional

To prospectively evaluate in a multicenter open label trial whether the use of zotarolimus-eluting ENDEAVOR Stent implantation in patients at low restenosis or at high bleeding or thrombotic risk will decrease the incidence of 12-month major adverse cardiac events (MACE) including overall death, any myocardial infarction (MI) or any target vessel revascularization (TVR).

NCT ID: NCT01384747 Terminated - Clinical trials for Coronary Artery Disease

Effect of Fimasartan for Modification of Atheroma Vulnerability in DEFERred Coronary Disease (FIMA-DEFER)

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

- Fimasartan will be more beneficial in stabilizing the plaque vulnerability compared to control group in deferred coronary lesions. - Fimasartan will be more beneficial in reducing total plaque volume compared to control group in deferred coronary lesions. - Fimasartan will be more beneficial in reducing functional impairment of stenotic lesions (assessed by FFR:Fractional Flow Reserve) in deferred coronary lesions.

NCT ID: NCT01384721 Recruiting - Clinical trials for Coronary Artery Disease

Computed Tomography Coronary Angiography (CTCA) Prognostic Registry for Coronary Artery Disease

PRORECAD
Start date: September 2010
Phase:
Study type: Observational

The study aims at pooling a large population of patients with suspected coronary artery disease (CAD) who underwent Computed Tomography Coronary Angiography (CTCA) and who were adequately stratified in the first place. Then the investigators will be able to assess the incremental value of CTCA in the stratification of prevalence of disease (non obstructive/obstructive) and prognosis of patients with suspected CAD). The added information to current evidence is how reliable and to what extent CTCA can define the actual burden of disease and cardiovascular risk.

NCT ID: NCT01384448 Completed - Clinical trials for Coronary Artery Disease

Stress Echocardiography and Heart Computed Tomography (CT) Scan in Emergency Department Patients With Chest Pain

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

The purpose of this study is to determine whether stress echocardiography or computed tomography (CT) of the heart is better at diagnosing emergency room chest pain patients to select appropriate candidates for hospitalization and further work-up.

NCT ID: NCT01384175 Completed - Clinical trials for Coronary Artery Disease

Epidural Anesthesia and Postoperative Analgesia With Ropivacaine and Fentanyl

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

The aim of the present study was to assess the efficacy of thoracic epidural anesthesia followed by postoperative epidural infusion and patient-controlled epidural analgesia with ropivacaine/fentanyl in off-pump coronary artery bypass grafting

NCT ID: NCT01383304 Active, not recruiting - Clinical trials for Coronary Artery Disease

Aspirin Response in High Risk Patients With Coronary Artery Disease

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

Previous studies indicate that patients with cardiovascular disease have a variable response to aspirin. Despite treatment with aspirin a large number of patients suffer a myocardial infarction. This has given rise to the phenomenon "aspirin low-responsiveness". Laboratory aspirin low-responsiveness can be defined as the failure of aspirin to inhibit platelet production of thromboxane A2 or inhibit thromboxane-dependent platelet aggregation. Whether a low platelet response to aspirin results in an increased risk of future thrombotic events is of great clinical significance, but is still unknown. The investigators hypothesize that patients with a reduced response to aspirin, determined by platelet aggregation using the apparatus Verify Now Aspirin and Multiplate, have a higher risk of thrombosis. The purpose of this study is to investigate whether a higher incidence of cardiovascular events is found in patients with coronary artery disease (CAD) having a reduced biochemical response to aspirin compared with CAD patients having a normal biochemical response to aspirin. In addition to CAD, all patients have at least one of the following risc factors: previous myocardial infarction, type 2 diabetes mellitus and/or renal insufficiency.

NCT ID: NCT01382277 Recruiting - Clinical trials for Coronary Artery Disease

Rosuvastatin Effect on Reducing Coronary Atherosclerosis Plaques Volume

REDUCT
Start date: March 2011
Phase: Phase 4
Study type: Interventional

This multicentre, open-label, single-arm Study is to evaluate the effect of Rosuvastatin 20 mg 76 weeks on coronary atherosclerosis plaque versus baseline in Chinese coronary heart disease (CHD) patients with hyperlipidemia by measuring the plaque volume using a 64 slice spiral CT. Effect on blood lipids, hsCRP and Carotid intima-media thickness (CIMT) is also evaluated.

NCT ID: NCT01380821 Completed - Clinical trials for Coronary Artery Disease

DNA Double-strand Breaks After SPECT

DSB-SPECT
Start date: March 2011
Phase: N/A
Study type: Observational

Ionizing radiation has a number of harmful effects in humans. The most important among these is the induction of cancer. It is assumed that damage to DNA in the nucleus of a single cell can induce cancer. Among the different types of lesions inducted, DNA double-strand breaks (DSBs) are considered to be the most relevant effects that can initiate carcinogenesis. The investigators are already conducting several other studies to prospectively compare the inducted DSBs by coronary CT-angiography and conventional coronary angiography. Extending these examinations to investigate the induced DSBs by myocardial scintigraphy allows a comparison of all three relevant imaging methods of the heart that incorporate ionizing radiation. To evaluate this, the investigators are planning to examine patients who are scheduled for a clinically indicated myocardial scintigraphy. These examinations are routinely done by the Department of Nuclear Medicine in either a 1-day or a 2-day protocol according to the diagnostic reference values of the Federal Department for Radiological Protection. Blood samples will be taken from these patients at predefined time steps before and after the examination and DNA double-strand breaks will be determined from these blood samples specifically considering the applied activity of the tracer and the exposition kinetics.

NCT ID: NCT01379677 Completed - Clinical trials for Coronary Artery Disease

Rubidium-82 PET and Tc-99m-MIBI SPET: A Head to Head Comparison

Start date: February 2011
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to compare myocardial perfusion imaging using Rubidium-82 PET with Tc-99m-MIBI SPET, in the evaluation of significant Coronary Artery Disease (CAD).