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Angina, Unstable clinical trials

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NCT ID: NCT03084367 Completed - Clinical trials for Coronary Artery Disease

Physiologic Assessment of Coronary Stenosis Following PCI

DEFINE PCI
Start date: June 20, 2017
Phase:
Study type: Observational

This is a pilot study designed to assess the relationship between iFR (instantaneous wave-free ratio) pullback and the distribution of coronary atheroma/stenoses as assessed by Quantitative Coronary Angiography (QCA) post angiographically successful PCI (Percutaneous Coronary Intervention).

NCT ID: NCT03083119 Recruiting - Clinical trials for Coronary Heart Disease

Efficacy and Safety of Xuesaitong Soft Capsule for Coronary Heart Disease Unstable Angina

Start date: March 20, 2017
Phase: Phase 2
Study type: Interventional

In this study, typical cases of coronary heart disease are selected. They will be intervened by Xuesaitong soft capsules to investigate efficacy and safety for Coronary Heart disease.

NCT ID: NCT03037047 Recruiting - Unstable Angina Clinical Trials

Efficacy and Safety of Salvianolate Injection in Elderly Patients With Unstable Angina Pectoris

Start date: May 11, 2016
Phase: Phase 4
Study type: Interventional

This parallel, double blind, randomized, controlled, multi-center study will evaluate the efficacy and safety of salvianolate injection in elderly patients with unstable angina pectoris.

NCT ID: NCT02983123 Completed - Clinical trials for Acute Coronary Syndrome

One-hour Troponin in a Low-prevalence Population of Acute Coronary Syndrome

OUT-ACS
Start date: November 15, 2016
Phase:
Study type: Observational

This study aims to evaluate if the 1-hour rule-in/rule-out algorithm for a high-sensitivity cardiac troponin T (hs-cTnT) is safe and effective for use in the primary care where the patients have a lower pretest probability of an acute myocardial infarction (MI). During this study troponins will be collected at 0-, 1- and 4/6-hours, where absolute changes in the values will decide whether the patient need hospitalization or not.

NCT ID: NCT02972814 Completed - Angina Pectoris Clinical Trials

Time Gain in the Diagnosis Myocardial Infarction by Troponin Point of Care Testing in the Emergency Room

T-POCT
Start date: February 1, 2017
Phase:
Study type: Observational

The investigators prospectively want to compare 3 clinical tests for measuring blood troponin levels in patients presenting to the emergency room with thoracic pain probably related to a myocardial infarction with regard to the time necessary to obtain the test results. The tests are one laboratory based test and two point of care tests.

NCT ID: NCT02939248 Completed - Clinical trials for Unstable Angina Pectoris

Influence of Naloxone on Ticagrelor Pharmacokinetics and Pharmacodynamics in Patients With Unstable Angina Pectoris on Concomitant Treatment With Morphine

Start date: October 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate differences in the pharmacokinetics and pharmacodynamics of ticagrelor and its active metabolite between patients who received ticagrelor and morphine followed by naloxone versus patients treated with ticagrelor and morphine alone for unstable angina pectoris.

NCT ID: NCT02939235 Completed - Clinical trials for Unstable Angina Pectoris

Influence of Metoclopramide on Ticagrelor Pharmacokinetics and Pharmacodynamics in Patients With Unstable Angina Pectoris on Concomitant Treatment With Morphine

Start date: July 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate differences in the pharmacokinetics and pharmacodynamics of ticagrelor and its active metabolite between patients who received ticagrelor and morphine followed by metoclopramide versus patients treated with ticagrelor and morphine alone for unstable angina pectoris.

NCT ID: NCT02925923 Completed - Clinical trials for Acute Coronary Syndrome

Crushed Ticagrelor Versus Eptifibatide Bolus + Clopidogrel

Start date: November 1, 2016
Phase: Phase 2
Study type: Interventional

Patients with troponin-negative acute coronary syndrome (ACS) are not routinely pre-treated with P2Y12 inhibitors and the rate of high on-treatment platelet reactivity (HPR) remains elevated after a loading dose of ticagrelor at the time of percutaneous coronary intervention (PCI). This suggests that faster platelet inhibition with crushed ticagrelor , eptifibatide , or cangrelor is needed to reduce HPR and periprocedural myocardial infarction and injury (PMI). The present study compared the effects of crushed ticagrelor vs. eptifibatide bolus + clopidogrel in troponin-negative ACS patients undergoing PCI.

NCT ID: NCT02893280 Withdrawn - Clinical trials for Acute Coronary Syndrome

Acute Coronary Syndrome Sri Lanka Audit Project

ACSSLAP
Start date: April 2015
Phase: N/A
Study type: Observational

ACSSLAP is the first island wide audit project in Sri Lanka on ACS.

NCT ID: NCT02868203 Not yet recruiting - Angina, Unstable Clinical Trials

OCT Based Edge and In-stent Vascular Response After Cordimax Stent in patIents With NSTE-ACS

Start date: August 2016
Phase: Phase 4
Study type: Interventional

This study evaluates the completeness of strut coverage and vessel wall response, at different time points (3-6-12 Months), following CordimaxTM stent implantation in patients with non-ST elevation acute coronary syndrome