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Coronary Artery Ectasia clinical trials

View clinical trials related to Coronary Artery Ectasia.

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NCT ID: NCT06057987 Recruiting - Clinical trials for Coronary Artery Ectasia

Coronary Artery Ectasia Database - Poland

CARED-POL
Start date: July 14, 2023
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to comprehensively investigate the current prevalence, morphological characteristics, risk factors for the development, complications as well as long-term prognosis of coronary artery aneurysm and ectasia (CAAE) in the Polish population. Data obtained from the CARED-POL Registry will enable the selection of morphological risk factors for the unfavorable course of CAAE, including the progression and development of giant aneurysms, aneurysm clotting with vessel occlusion, and thromboembolic complications. Comparing the safety and effectiveness of available CAAE treatment methods in individual patient subgroups will allow individualization of treatment, including anticoagulant therapy.

NCT ID: NCT05713201 Recruiting - Coronary Disease Clinical Trials

Outcomes After PCI of the Aneurysmatic Right Coronary Artery

RIGHT-MARE
Start date: November 1, 2022
Phase:
Study type: Observational

This study aims to evaluate procedural and clinical outcomes of acute coronay syndrome (ACS) patients with aneurysmatic culprit right coronary artery (RCA).

NCT ID: NCT05233124 Recruiting - Clinical trials for Acute Coronary Syndrome

Antithrombotic Therapy in Acute Coronary Syndromes and Coronary Artery Ectasia

OVER-TIME
Start date: September 1, 2021
Phase: Phase 2
Study type: Interventional

The optimal anti-thrombotic therapy to prevent recurrent ischemic events in patients with acute coronary syndrome and coronary artery ectasia (CAE) remains unclear. OVER-TIME is an investigator initiated, exploratory, open label, single center, randomized clinical trial comparing dual antiplatelet therapy (acetyl-salicylic acid plus a P2Y12 inhibitor) with the combination of an antiplatelet monotherapy (a P2Y12 inhibitor) plus a low dose anticoagulant (rivaroxaban, 15mg oral dose) for the prevention of recurrent ischemic events among patients with CAE. The investigators aim to enroll 60 patients with CAE and acute coronary syndromes. After recruitment, patients are randomized to (a) standard of care (dual antiplatelet regimen) or (b) the combination of antiplatelet monotherapy and low dose anticoagulant. Patients will be followed for at least 12 months. The OVER-TIME study aims to assess the efficacy of the regimen in prevention of major cardiovascular events and its security in bleeding events in acute coronary syndromes among patients with CAE. OVER-TIME is the first randomized controlled trial to assess different antithrombotic strategies in patients with CAE and acute coronary syndrome, and its results will offer preliminary data for the prevention of major cardiovascular events and bleeding events in this group of patients.

NCT ID: NCT05106530 Recruiting - Clinical trials for Coronary Artery Ectasia

Arrhythmogenic Risk Assessment in Coronary Artery Ectasia Patients

Start date: January 1, 2022
Phase:
Study type: Observational [Patient Registry]

The investigators thought to explore arrhythmias outcome - hidden arrhythmias, ECG features: Tp-Te interval and Tp-Te/QTc ratio, fQRS among patients with coronary artery ectasia as compared to normal coronary artery patients.

NCT ID: NCT04265989 Recruiting - Clinical trials for Coronary Artery Ectasia

A New Classification and Interventional Therapy for Coronary Artery Ectasia

NCIPCAE
Start date: November 1, 2019
Phase: N/A
Study type: Interventional

This study is aim to present a new classification for coronary artery ectasia and find the best interventional therapy for different types of patients were treated and studied.

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: NCT00548457 Recruiting - Clinical trials for Coronary Artery Ectasia

Endothelial Function in Patients With Ectatic Compared to Normal Coronary Arteries

Start date: May 2006
Phase: N/A
Study type: Observational

The aim of this study is to show the frequency of endothelial dysfunction in patients suffering from ectatic coronary arteries as compared to those who have normal coronary arteries. Should this frequency be significant we would recommend initiating conventional treatment in those patients with ectatic coronary arteries as is the practice in patients with endothelial dysfunction without ectatic arteries