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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT02070159 Completed - Clinical trials for Coronary Artery Disease

Prasugrel With Lower Dose - Loading Dose

PRELOAD-LD
Start date: December 2011
Phase: Phase 3
Study type: Interventional

Although prasugrel, recently available thienopyridine derivative, exhibits rapid and potent platelet inhibition, concerns of low on-treatment platelet reactivity have been suggested especially in East Asian ethnicities. The investigators compared the effect of lower loading dose of prasugrel with conventional loading dose of clopidogrel and prasugrel.

NCT ID: NCT02069405 Completed - Clinical trials for Patients Undergoing Coronary CT Angiogram

Relaxation Music to Lower Heart Rate Prior to Cardiac CT

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

To acquire low radiation dose and good quality cardiac CT images requires scanning at low heart rates which is usually done with beta-blockers. However, in some patients beta-blockers have little effect. This is thought to be due to a different mechanism of action which continues to maintain the heart rate despite administration of beta-blockers. This study aims to look at the effect of music or relaxation tracks to reduce patient heart rate as anxiety is thought to play a role in maintaining high heart rates. This study will randomise patients into a normal standard of care group compared to a normal standard of care group with music/ relaxation track and compare heart rate, radiation dose, image quality, amount of beta-blocker used and patient experience via a State-Trait Anxiety Inventory (STAI) questionnaire.

NCT ID: NCT02065479 Completed - Clinical trials for Coronary Artery Disease

A Pharmacodynamic Study Comparing Prasugrel Versus Ticagrelor in Patients Undergoing PCI With CYP2C19 Loss-of-function:

Start date: March 2014
Phase: Phase 4
Study type: Interventional

Numerous studies have shown that pharmacodynamics (PD) response profiles vary among clopidogrel treated patients and that individuals with reduced response have an increased risk of recurrent ischemic events. There are multiple factors contributing to clopidogrel response variability, including genetic variations of the cytochrome P450 (CYP) 2C19 enzyme. In particular, loss-of-function (LOF) alleles of the CYP2C19 enzyme reduce transformation of clopidogrel pro-drug into its active metabolite. Thus, patients carrying LOF alleles have lower levels of clopidogrel's active metabolite as well as diminished platelet inhibition, which translates into an increased rate of adverse cardiovascular events, particularly in the setting of percutaneous coronary intervention (PCI). Prasugrel and ticagrelor are novel generation P2Y12 receptor inhibitors characterized by greater PD potency and reduced ischemic event rates compared with clopidogrel, and are not affected by CYP2C19 LOF polymorphisms. However, to date there are limited head-to-head PD comparisons between these two new P2Y12 receptors blockers, and there are no studies assessing on how these agents behave among CYP2C19 LOF carriers. The aim of the present study is to compare the PD effects of prasugrel versus ticagrelor in patients undergoing PCI with CYP2C19 LOF alleles using the novel point-of-care genetic testing Spartan RX-CYP2C19 which permits accurate and rapid identification of CYP2C19 genetic status.

NCT ID: NCT02064985 Completed - Clinical trials for Stable Coronary Heart Disease (CHD)

Ticagrelor China Pharmacokinetic/Pharmacodynamic Study

Start date: February 2014
Phase: Phase 4
Study type: Interventional

open label, single centre, randomised, Phase IV, pharmacokinetic, pharmacodynamic, and safety study to evaluate single and multiple doses of 45, 60, and 90 mg of ticagrelor in Chinese patients with stable coronary heart disease

NCT ID: NCT02063347 Recruiting - Clinical trials for Coronary Artery Disease

Innate Human Collateral Supply to Different Vascular Regions

Start date: November 2013
Phase: N/A
Study type: Observational

Both clinical and experimental studies demonstrate the importance of the pre-existing, ie innate collateral supply in different vascular regions. Furthermore, pathophysiological considerations and experimental data imply an important role for the association of collateral function between different vascular regions. STUDY HYPOTHESES 1. In the absence of atherosclerotic stenoses, there is a direct association between the collateral function in the coronary, renal and peripheral circulation. 2. The increase in plasma renin in response to a unilateral main renal artery balloon occlusion is inversely related to its functional collateral supply. 3. The decrease in renal vein oxygen saturation in response to a unilateral main renal artery occlusion is inversely related to its functional collateral supply.

NCT ID: NCT02062424 Completed - Clinical trials for Ischemic Heart Disease

Diet and Prevention of Ischemic Heart Disease: a Translational Approach

DIPI
Start date: February 2014
Phase: N/A
Study type: Interventional

The objective of this study is to test the effect of substitution dietary guidelines that are specifically aimed at the prevention of ischemic heart disease (IHD) on the dietary intake in the general Danish population.

NCT ID: NCT02062216 Not yet recruiting - Clinical trials for Coronary Artery Disease

Role of the Inflammatory Receptors in the Pathogenesis of Atherosclerosis

Receptors
Start date: February 2015
Phase: N/A
Study type: Observational

The primary objective of this study is to assess whether inflammatory receptors play a role in the pathogenesis of atherosclerosis.

NCT ID: NCT02061891 Active, not recruiting - Clinical trials for Coronary Artery Disease

Very Early veRsus Deferred Invasive Evaluation Using Computerized Tomography in Patients With Acute Coronary Syndromes

VERDICT-EDI
Start date: November 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate if acute invasive coronary evaluation and treatment conducted within 12 hours of diagnosis improves clinical outcome compared to a deferred, subacute strategy in patients with unstable angina pectoris (UAP) / non-ST segment elevation myocardial infarction (NSTEMI) Acute coronary syndrome (ACS) Furthermore, in an observational design the potential clinical benefit of coronary computed tomography angiography (CCTA) to select patients for invasive investigation and treatment in the two treatment arms (acute vs deferred) is evaluated. The following main hypothesis will be tested: - Very early invasive coronary investigation improves clinical outcome in patients with UAP/NSTEMI-ACS - CCTA performed before invasive coronary investigation will improve clinical management of patients with UAP/NSTEMI-ACS

NCT ID: NCT02061696 Terminated - Clinical trials for Coronary Artery Disease

ARISTOCRAT-A Randomized Controlled Trial Evaluating Closure Following Access With the AXERA (Device Name) 2 Access System

ARISTOCRAT
Start date: January 2014
Phase: N/A
Study type: Interventional

The goal of the research study is to observe the clinical safety, effectiveness and patient satisfaction of the AXERA 2 Access System in subjects undergoing coronary angiographic and possible Percutaneous Coronary Intervention (PCI) through the femoral artery when compared to standard manual compression.

NCT ID: NCT02060968 Completed - Clinical trials for Coronary Artery Disease

IRIS-PREMIER REGISTRY

IRIS-PREMIER
Start date: August 2014
Phase:
Study type: Observational

The purpose of this study is to evaluate effectiveness and safety of Promus PREMIER in Routine Clinical Practice