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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT04004832 Recruiting - Clinical trials for Coronary Artery Disease With Myocardial Infarction

Comparison of the Severity of Coronary Atherosclerosis With Tissue Compliance in Patients Within First Degree Relatives

Start date: September 18, 2020
Phase:
Study type: Observational

This study research the similarity of coronary artery lesions according to HLA tissue compatibility in fisrt degree relatives of the patients who just admitted clinic as Acute coronary syndrome and underwent angiyography before .

NCT ID: NCT04004546 Recruiting - Coronary Disease Clinical Trials

Improving Medication Adherence Through a Health Literacy-based Intervention for Coronary Heart Disease Patients

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

This is a multi-center pilot study to examine the effectiveness of a health literacy-based intervention to improve medication adherence and self-efficacy of medication use among individuals with coronary heart disease (CHD). The specific aims are to: i) develop a health literacy-based intervention to improve medication adherence for CHD individuals with low health literacy and ii) evaluate the effects of a health literacy-based intervention on improving medication adherence and self-efficacy in CHD individuals.

NCT ID: NCT04001894 Completed - Platelet Reactivity Clinical Trials

Ticagrelor and Clopidogrel on Platelet Effects in Chinese Patients With Stable Coronary Artery Disease

Start date: July 2, 2019
Phase: Phase 4
Study type: Interventional

Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor reduces thrombotic events in patients with coronary artery disease, but these benefits come at the expense of increased risk of bleeding when compared with aspirin monotherapy. Increased evidence showed that P2Y12 inhibitor monotherapy still maintain antiischemic efficacy while reducing the bleeding risk compared with DAPT. Therefore, the investigators performed this study to observe the efficacy of ticagrelor in comparison to clopidogrel in Chinese patients with stable CAD.

NCT ID: NCT04001452 Not yet recruiting - Clinical trials for Coronary Artery Disease

2nd International Survey on Interventional Strategies

Start date: July 1, 2019
Phase:
Study type: Observational

The study aims to evaluate the decision-making pathways of interventional cardiologists, when assessing patients, presented with stable coronary artery disease.

NCT ID: NCT04001283 Recruiting - Clinical trials for Coronary Artery Disease

Nitrite Effects on Cardiac Muscle in CABG

Start date: January 21, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test whether sodium nitrite affects the expression of cellular proteins important for metabolic and vascular function in vascular offcuts and cardiac biopsies taken from patients undergoing coronary artery bypass grafting (CABG) surgery.

NCT ID: NCT03999463 Completed - Clinical trials for Ischemic Heart Disease

Sevoflurane Effect on Left Atrial Performance: A Transoesophageal Echocardiographic Study

Start date: July 1, 2019
Phase:
Study type: Observational [Patient Registry]

The left atrial performance is affected by the preload as well as the afterload. The LA active pumping is increased by stretching of the LA but within limits, after which the active pumping declines. The LV stiffness acts as the LA afterload. Whenever the LV stiffness increases, the overall emptying fraction becomes more pumpdependent

NCT ID: NCT03997201 Completed - Clinical trials for Ischemic Heart Disease

Ripple Mapping Guided Ablation of Ischaemic Ventricular Tachycardia.

RIPPLE-VT
Start date: April 18, 2019
Phase: N/A
Study type: Interventional

The Ripple VT-1 Study is a prospective clinical trial that aims to investigate if catheter ablation of ventricular tachycardia in patients with ischaemic heart disease can be effectively performed using Ripple Mapping.

NCT ID: NCT03988166 Completed - Clinical trials for Ischemic Heart Disease

Chronic Total Occlusion Percutaneous Coronary Intervention Study

CTO-PCI
Start date: May 20, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate angiographic confirmation of placement of any guidewire beyond the CTO, in the true vessel lumen, in patients undergoing CTO percutaneous coronary intervention (PCI) in which at least one Teleflex guidewire and at least one Turnpike catheter are used.

NCT ID: NCT03986697 Not yet recruiting - Clinical trials for Coronary Artery Disease

How Does Antiretroviral Therapy Affect Coronary Atherosclerosis: A Serial CT Study

HART CT
Start date: November 4, 2019
Phase: Phase 4
Study type: Interventional

Combined antiretroviral therapy (cART) is thought to promote coronary artery disease via a number of mechanisms: abnormal lipid profiles, endothelial dysfunction, hypertension, insulin resistance and renal impairment are the main pathological mechanisms driving atherosclerosis as a consequence of cART. An association between protease inhibitors and increased cardiovascular disease risk has been shown in many large cohort trials. CT Coronary Angiography (CTCA) is now widely used to assess for the presence of atherosclerosis, typically in patients presenting with chest pain. This imaging technique allows visualisation of the coronary arteries and quantification of any atherosclerotic disease that may be present. This technique is being increasingly used as a surrogate for cardiovascular disease risk. HART CT is an open label, prospective, randomised-control pilot study to investigate the feasibility of performing a future appropriately powered multi-centred randomised control trial using CT based outcome data as a surrogate for cardiovascular disease risk. Participants will be randomised to either continue their usual cART or switch to Biktarvy (a fixed dose combination of bictegravir, emtricitabine and tenofovir alafenamide). A baseline CT scan will be performed. If there is any evidence of atherosclerosis a further CT scan will be performed at the end of the study (approximately 48 weeks). This will allow quantification of any change in coronary artery plaque burden or characteristic. Participants will be also followed up for any changes in metabolic health.

NCT ID: NCT03985241 Completed - Clinical trials for Coronary Artery Disease

Functional Assessment of Myocardial Ischemia by Intracoronary Electrocardiogram

FFRicECG
Start date: December 3, 2016
Phase: N/A
Study type: Interventional

In patients with chronic stable coronary artery disease (CAD), percutaneous coronary intervention (PCI) targets hemodynamically significant coronary lesions, i.e., those thought to cause inducible ischemia. The hemodynamic severity of a coronary stenosis increases with its tightness and with the myocardial mass of viable myocardium downstream of the stenosis. Compared to the traditional anatomic angiographic approach, assessment of functional relevance by fractional flow reserve (FFR) during coronary angiography has been suggested to improve patient outcomes. Fractional flow reserve (FFR) is based on determination of the coronary perfusion pressure downstream of a stenosis during pharmacologic hyperemia. However, FFR relies on oversimplified physiologic concepts, which limits its usefulness in defining a true ischemic threshold. Furthermore, visual angiographic assessment continues to dominate the treatment decisions for intermediate coronary lesions. Conversely, the intracoronary ECG (icECG) provides an inexpensive, sensitive and direct measure of myocardial ischemia. The icECG is easily acquired by attaching a reusable alligator clamp to a conventional angioplasty guidewire (at one tenth the price of a pressure sensor guidewire). The coronary guide wire positioned downstream of a coronary stenosis then acts as the exploring electrode. During pharmacologic stress, the icECG can provide direct evidence for regional myocardial ischemia to define the ischemic threshold in different types of coronary artery disease.