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Infarction clinical trials

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NCT ID: NCT05949515 Completed - Clinical trials for Acute ST Segment Elevation Myocardial Infarction

Retrospective Evaluation of SuperSaturated Oxygen (SSO2) Therapy Clinical Utility

RESCU
Start date: July 31, 2023
Phase:
Study type: Observational

The purpose of this multicenter study is to assess the impact of SSO2 treatment on clinical outcomes and left ventricular function in patients following acute ST-segment elevation myocardial infarction (STEMI).

NCT ID: NCT05895123 Completed - Clinical trials for ST-segment Elevation Myocardial Infarction

Comparison Between the Effects of High Doses Statin on Ventricular Remodeling in STEMI Patients

Start date: October 1, 2022
Phase: Phase 2
Study type: Interventional

STEMI is a serious type of coronary heart disease, which is a major cause of disability and death. Morphologically the key feature of remodeling is myocyte hypertrophy, myocyte loss from necrosis or apoptosis, as well as interstitial cell growth especially fibroblast proliferation leading to myocardial fibrosis . Elevated serum LDL-cholesterol concentrations play a proatherogenic role by stimulating inflammation and oxidative processes. Statins have been documented to retard fibrosis and ventricular hypertrophy by the cessation of myofibroblast activity. Clinical studies have proven that statins not only regulate lipids but also improve myocardial fibrosis, regulate cell proliferation and apoptosis, regulate ventricular remodeling, and protect the myocardium

NCT ID: NCT05894330 Completed - Clinical trials for Stroke, Middle Cerebral Artery With Infarction, Rehabilitation, Upper Limb Recovery, Economic Burdon

Perception About Upper Limb Functional Recovery, Barriers & Use of Training Devices Among Indian Stroke Survivors.

Start date: August 1, 2021
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to evaluate perceptions regarding affected arm and hand function and their willingness to use devices to enhance upper limb functions among stroke survivors. The main question[s] it aims to answer are: - what will the stroke survivor's perception of interventions and device development in his/her arm recovery? - Wheather he is willing to use it for his arm recovery?

NCT ID: NCT05849805 Completed - Clinical trials for Stroke, Acute Ischemic

Y-3 Injection Through Skull Bone Marrow in the Treatment of Acute Malignant Middle Cerebral Artery Infarction (SOLUTION)

Start date: April 17, 2023
Phase: N/A
Study type: Interventional

The mortality of malignant middle cerebral artery infarction (mMCAI) is up to 80%, while current available treatment is limited. The purpose of this study is to explore the feasibility, safety and efficacy of Intracalvaria bone marrow injection of cytoprotective drug Y-3 in mMCAI patients with contradictions of reperfusion therapy or poor reperfusion outcome.

NCT ID: NCT05843006 Completed - Clinical trials for Acute Myocardial Infarction

Sweat Analysis as Prognosticator After Heart Attack

SWEATHEART
Start date: March 21, 2022
Phase:
Study type: Observational [Patient Registry]

This study characterizes non-invasive body inflammation response in sweat and blood of patients suffering from acute myocardial infarction and explores the potential of non-invasive sweat analysis a an innovative approach for predicting patient outcome.

NCT ID: NCT05748691 Completed - Heart Failure Clinical Trials

Switching From Cardiac Troponin I to T

TWITCH-ED
Start date: October 25, 2020
Phase:
Study type: Observational

Cardiac troponin is central to the diagnosis of myocardial infarction and high-sensitivity cardiac troponin (hs-cTn) assays are the preferred choice for the assessment of patients with suspected acute coronary syndrome. Since the introduction of hs-cTn assays in Europe in 2010, most hospitals have switched from contemporary sensitive cardiac troponin assays to a hs-cTn assay. The implementation of hs-cTn assays has led to an increase in the number of patients identified with myocardial injury. Although both hs-cTnI and hs-cTnT assays are recommended in current guidelines, the impact of switching from a hs-cTnI assay to a hs-cTnT assay on clinical practice is unknown. At this point, no studies have evaluated the impact of implementing sex-specific hs-cTnT thresholds on the diagnosis of myocardial infarction and outcome in clinical practice. The investigators propose to determine the proportion of patients with and without myocardial injury admitted to the hospital before and after implementation of a hs-cTnT assay and to evaluate the impact on investigations, care and clinical outcomes in consecutive patients with suspected acute coronary syndrome.

NCT ID: NCT05733507 Completed - Clinical trials for Paramedian Pontine Infarction (IPP)

Tirofiban Plus Intravenous Thrombolysis in Acute Anterior Choroidal Infarction or Paramedian Pontine Infarction

TITACIPPI
Start date: April 3, 2023
Phase:
Study type: Observational

TITACIPPI (Tirofiban with Intravenous Thrombolysis in Acute Anterior Choroidal Infarction [ACI] and Paramedian Pontine Infarction [IPP]) study aimed to evaluate the efficacy and safety of simultaneous infusion of tirofiban with intravenous thrombolysis (IVT + tirofiban group) compared to IVT alone (IVT alone group) in patients with ACI or PPI. TITACIPPI study is a retrospective, single-center observational study conducted from March 01, 2014, to December 31, 2022.

NCT ID: NCT05732324 Completed - Clinical trials for Coronary Artery Disease

Comparison of Percutaneous Coronary Intervention Optimization With Fractional Flow Reserve Versus Intravascular Ultrasound in the Treatment of Long Coronary Artery Lesions

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

A single center, prospective, observational study to compare fractional flow reserve (FFR) and intravascular ultrasound (IVUS) percutaneous coronary intervention (PCI) optimization strategies on the functional PCI result (assessed with FFR) immediately post PCI and at 9-12 months after the treatment of long coronary artery lesions.

NCT ID: NCT05705089 Completed - Clinical trials for ST Segment Elevation Myocardial Infarction

Rivaroxaban vErsus Warfarin for Antithrombotic TheRapy in Patients With LeFt Ventricular Thrombus After Acute STEMI

REWARF-STEMI
Start date: July 30, 2020
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the safety and efficacy of rivaroxaban-based versus warfarin-based antithrombotic regimens on outcomes of patients with left ventricle thrombosis following acute ST elevation myocardial infarction at 3 months from enrollment in an open-label parallel groups pilot randomized clinical trial

NCT ID: NCT05704569 Completed - Stroke Clinical Trials

Prediction of Primary Cardiovascular Events Using the Multimarker Approach

Start date: June 1, 2014
Phase:
Study type: Observational

The study of biochemical risk factors for cardiovascular diseases is important not only for analysis, but also for preventive measures, given that changes in the level of biomarkers can be detected before the first clinical manifestations of CVD. Accordingly, patients at high CV risk may have additional motivation to lead a healthy lifestyle. In addition, information on biochemical risk markers can be used to optimize the clinical management of patients.