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Coronary; Ischemic clinical trials

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NCT ID: NCT05868902 Recruiting - Coronary; Ischemic Clinical Trials

A Registry of Cardiac PET and CardioFlux Magnetocardiography in Patients With Suspected Coronary Ischemia.

Magneto-PET
Start date: August 28, 2023
Phase:
Study type: Observational

A multicenter observational data development registry collecting diagnostic measures via standard of care (SOC) cardiac PET in order gain a better understanding of how CardioFlux MCG may be used in the detection of coronary ischemia.

NCT ID: NCT05308329 Recruiting - Clinical trials for Acute Coronary Syndrome

Kitasato PCI Registry

Start date: February 1, 2012
Phase:
Study type: Observational

The Kitasato PCI Registry is a single-center, observational, prospective study. This study aims to investigate the impact of characteristics in clinical manifestation, patients' background, procedure of percutaneous coronary intervention (PCI), and pre/post PCI culprit/nonculprit lesion observed by intra-coronary imaging modality on clinical outcomes.

NCT ID: NCT05197361 Active, not recruiting - Clinical trials for Chronic Total Occlusion of Coronary Artery

Microvascular Coronary Resistance and Absolute Coronary FLOW in Patients With Percutaneous Intervention of a Chronic Total Occlusion

FLOW-CTO
Start date: October 1, 2020
Phase:
Study type: Observational

It is an observational study which objective is to analyze, through a series of invasive parameters, the state of the coronary microvasculature immediately after the successful percutaneous coronary intervention of a chronic total occlusion and at 6 months after the index procedure. The aim of the study is to check the variation in the values of the index of microcirculatory resistance (IMR) and invasive absolute coronary flow (AF). The working hypothesis is that, in the follow-up of these patients, AF will increase significantly with respect to its baseline and, conversely, IMR will be reduced during the follow-up.

NCT ID: NCT04827316 Recruiting - Clinical trials for Coronary Artery Disease

Clinical Utility and Outcome Prediction of Cardiovascular Computed Tomography (PREDICT-CT)

PREDICT-CT
Start date: June 1, 2017
Phase:
Study type: Observational [Patient Registry]

In this study the investigators retrospectively and prospectively collect information from enrolled subjects undergoing CCTA and evaluate the association of cardiac and non-cardiac imaging with laboratory markers and clinical data including outcome.

NCT ID: NCT04674449 Recruiting - Clinical trials for Coronary Artery Disease

iCorMicA - Stratified Medicine in Angina

iCorMicA
Start date: December 30, 2020
Phase: N/A
Study type: Interventional

The iCorMicA study is a multicentre, prospective, randomised, double-blind, sham-controlled, parallel-group, end-point trial and registry. The investigators seek to determine whether stratified medical therapy guided by an adjunctive interventional diagnostic procedure (IDP) during the invasive management of patients with known or suspected angina but no obstructive coronary artery disease improves symptoms, wellbeing, cardiovascular risk and clinical outcomes.

NCT ID: NCT04664439 Recruiting - Coronary; Ischemic Clinical Trials

Follow-up With CT-FFR in CHD Patients After DCB

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

In recent years, based on CCTA data, CT-derived fractional flow reserve (CT-FFR) developed by artificial intelligence and other technologies can provide both anatomical and functional information of coronary artery disease. Compared with CCTA alone, CT-FFR has a better ability to diagnose coronary ischemic lesions and can effectively reduce the need for unnecessary ICA, to predict revascularization more accurately.

NCT ID: NCT03894176 Completed - STEMI Clinical Trials

Association of Plasma PTX3 Concentration and Outcomes of STEMI

Start date: January 1, 2018
Phase:
Study type: Observational

335 of patients with STEMI treated by primary PCI were assayed for PTX3 measurement by ELISA method. The angiographic and clinical outcomes were evaluated according to the PTX3 concentration.

NCT ID: NCT03461705 Terminated - Coronary; Ischemic Clinical Trials

Novel Adenosine-independent Index of Coronary Artery Stenosis Severity Resting Flow Reserve

RFR
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

This study will enroll patients who are referred for coronary angiography and require physiological assessment to see if the lesion can be treated as per the local standard of care. Approximately 92 participants will be enrolled. There are no follow up visits required so participation in this study will end when subjects are discharged from the hospital.The study will be comparing the resting flow reserve against the instantaneous wave-free ratio (iFR) and fractional flow reserve. All these tests offer a way to image a legion and determine if it is suitable to be treated. FFR measures the pressure differences across (narrowed coronary arteries usually due to atherosclerosis), iFR's are performed during cardiac catheterisation (angiography) using invasive coronary pressure wires which are placed in the arteries of the heart that are to be assessed and the Resting flow reserve looks at the maximum increase in blood flow through the coronary arteries above the normal resting volume.

NCT ID: NCT02668250 Completed - Stroke Clinical Trials

Influence of a Multi-parametric Optimization Strategy for General Anesthesia on Postoperative Morbidity and Mortality

OPTI-AGED
Start date: February 3, 2017
Phase: N/A
Study type: Interventional

With the increasing aging population demographics and life expectancies, the number of very elderly patients undergoing surgery is rising. Elderly patients constitute an increasingly large proportion of the high-risk surgical group. Cardiac complications and postoperative pulmonary complications are equally prevalent and contribute similarly to morbidity, mortality, and length of hospital stay. Specific optimization strategy of general anesthesia has been tested in high-risk patients undergoing major surgery to improve outcomes. Our hypothesis is that a combined optimization strategy of anesthesia concerning hemodynamic, ventilation, and depth of anesthesia may improve short- and long- term outcome in elderly undergoing high risk surgery.