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No-Reflow Phenomenon clinical trials

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NCT ID: NCT03296670 Completed - Clinical trials for ST Segment Elevation Myocardial Infarction

Efficacy of Intracoronary Infusion of Different Medicine in STEMI Patients With CSFP

Start date: August 1, 2015
Phase: Phase 4
Study type: Interventional

The study intends to evaluate the efficacy of different medicine delivering by targeted perfusion catheter in coronary administration on coronary blood flow in STEMI patients with CSFP.

NCT ID: NCT03264859 Not yet recruiting - Clinical trials for STEMI - ST Elevation Myocardial Infarction

NGAL and Its Association With the No-reflow Phenomenon in ST-elevation Myocardial Infarction

Start date: September 15, 2017
Phase: N/A
Study type: Observational

The aim of this study is to investigate the association between NGAL plasma levels in ST-elevation myocardial infarction and the no-reflow phenomenon, adverse events during hospitalization and at 30-day follow-up.

NCT ID: NCT02831153 Recruiting - Depression Clinical Trials

Evaluation of Emotional Status and Coronary Flow Characteristics by TIMI Frame Count Method

STRAIN-TIMI
Start date: July 2016
Phase: N/A
Study type: Interventional

This study evaluates the effects of emotional status on coronary flow in patients undergoing elective coronary angiography. Patients whom undergoing elective coronary angiography will fulfill the Beck Anxiety Inventory, Beck Depression Inventory, State-Trait Anxiety Inventory, Hospital Anxiety and Depression Scale. State Anxiety Inventory will be fulfilled both before the intervention and after 1 hour the patients learned the results of the coronary angiography. The other scales will be performed after 1 hour the patients learned their results. Coronary flow will be assessed by TIMI (Thrombolysis In Myocardial Infarction) frame count method.

NCT ID: NCT02818127 Recruiting - Clinical trials for Coronary Artery Disease

Assessment Of Total Coronary Circulation Time Using TIMI Frame Count Method (TCCT-TIMI)

TCCT-TIMI
Start date: July 2016
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate and describe the total coronary circulation time (TCCT) by using TIMI frame count method in patients performed coronary angiography. TCCT is described as an angiographic index which is the sum of the frame count of coronary artery and venous system. This study also evaluates the relationship between the diseases in arterial system such as coronary artery ectasia, coronary slow flow, coronary artery disease and coronary venous pathologies.

NCT ID: NCT02233790 Not yet recruiting - Clinical trials for Myocardial Infarction

Ticagrelor and Clopidogrel on Reperfusion in Patients With AMI

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

The patients with acute myocardial infarction (AMI) present high mortality and morbidity rate,even treated with stenting in the blocked heart vessels. The appearance of no-reflow is common after re-opening of the blocked vessel. The no-reflow were commonly attributed to tiny blockage in coronary micro-vasculature by thrombus and spasm of the micro-vessel during stenting. An agent with more effective anti-clotting and micro-vessel dilation would be helpful to solve the issue of no-reflow. Ticagrelor was demonstrated to be a potent platelet inhibitor and a potent micro-vessel dilator which can influence metabolism of adenosine, a endogenous potent small vessel dilator. This study is to test the effectiveness of ticagrelor on improving reperfusion and minimizing the myocardial infarct size after PPCI in patients with AMI.

NCT ID: NCT02054000 Completed - Clinical trials for No-Reflow Phenomenon

Intracoronary Tirofiban on No-Reflow Phenomena

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

The goal of this study was to evaluate the acute effect of intracoronary administration of tirofiban on no-reflow phenomenon in patients with STEMI and occurrence of no-reflow phenomenon undergoing primary percutaneous coronary intervention (PCI).

NCT ID: NCT01430884 Recruiting - Clinical trials for Coronary Heart Disease

Analysis of Human Coronary Aspirate

AHCA
Start date: April 2004
Phase: N/A
Study type: Observational

During elective percutaneous coronary intervention (PCI), both proximal and distal protection devices are used. The distal occlusion protection device temporarily occludes the vessel distal to the lesion during the intervention, thereby capturing both particular debris and soluble substances released from the lesion such that they can be aspirated and prevented from reaching the coronary microcirculation. Rather than simply discarding the material which is retrieved from use of protection devices, the investigators have recently taken advantage of this situation, sampled the particulate and soluble material and subjected it to a variety of analyses with the ultimate goal to have a better insight into the respective plaque composition and to correlate it to the individual imaging and clinical data. On the basis of such information the investigators aim to better understand the pathophysiology of plaque vulnerability and to possibly predict the clinical development of the individual patient.