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Infarction clinical trials

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NCT ID: NCT03947619 Recruiting - Clinical trials for ST Elevation (STEMI) Myocardial Infarction of Anterior Wall

Primary Unloading and Delayed Reperfusion in ST-Elevation Myocardial Infarction: The STEMI-DTU Trial

DTU-STEMI
Start date: December 12, 2019
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate whether using the the IMPELLA® CP System temporary circulatory assist device for 30 minutes prior to a catheterization procedure has the potential to reduce the damage to the heart caused by a heart attack, compared to the current standard of care.

NCT ID: NCT03940443 Recruiting - Clinical trials for Traumatic Brain Injury

Differences in Mortality and Morbidity in Patients Suffering a Time-critical Condition Between GEMS and HEMS

Start date: September 3, 2019
Phase:
Study type: Observational

Introduction: Patients suffering a time-critical medical condition require rapid prehospital assessment and treatment and most often quick transportation to definitive care. This can be decisive for patient outcome. In order to minimize time from assessment to treatment, thus lowering mortality and morbidity, it is important to have a well-coordinated chain of care. The efficient use of Ground Emergency Medical Services (GEMS) and Helicopter Emergency Medical Services (HEMS) is essential in such a chain of care. Objectives: The aim is to describe differences in mortality, morbidity, assessment and treatment of two time-critical conditions, traumatic brain injury (TBI) and acute myocardial infarction (MI), in patients assessed by GEMS and HEMS respectively. Method: The project consists of a descriptive observational study and comparative cohort study. Inclusion criteria are patients considered to be suffering from TBI and acute MI, which are treated by GEMS or HEMS in the regions of Uppsala, Jämtland/Härjedalen, Dalarna and Värmland. Clinical significance: The results expect to be the basis for further studies aiming to optimize the utilization of GEMS and HEMS.

NCT ID: NCT03939338 Recruiting - Clinical trials for STEMI - ST Elevation Myocardial Infarction

Combination With Treg Levels and CMR to Assess the Severity and Prognosis of Reperfusion Injury After PPCI in STEMI Patients

TregCMRRS
Start date: July 1, 2019
Phase:
Study type: Observational

This study aims to determine whether combination with regulatory T cell (Treg) levels and cardiac magnetic resonance imaging (CMR) are predictive of the severity of reperfusion injury following myocardial infarction and the prognosis in STEMI patients receiving primary percutaneous coronary intervention (PPCI).

NCT ID: NCT03933358 Recruiting - STEMI Clinical Trials

Effect of Thyroid Hormone on Post-Myocardial Infarction Remodeling and Prognosis in STEMI Patients

ThyREST
Start date: May 1, 2019
Phase:
Study type: Observational

This study aims to determine whether thyroid hormone levels are predictive of cardiac remodeling following myocardial infarction and the prognosis in patients with STEMI receiving primary percutaneous coronary intervention.

NCT ID: NCT03932084 Recruiting - Clinical trials for Type 2 Diabetes and Cerebral Infarction

Effects of Glucose Fluctuation Intervention on the Prognosis of Patients With Type 2 Diabetes and Cerebral Infarction

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The present randomized control trial sought to establish glucose fluctuation as an important target for management on metabolic index, neurologic function, and quality of life in Type 2 diabetes mellitus (T2DM) patients and cerebral infarction (CI).

NCT ID: NCT03920176 Recruiting - Clinical trials for Cardiovascular Diseases

Computed Tomography Coronary Angiography for the Prevention of Myocardial Infarction (The SCOT-HEART 2 Trial)

SCOT-HEART 2
Start date: January 13, 2020
Phase: N/A
Study type: Interventional

It is hypothesised that, in individuals being considered for cardiovascular preventative therapy, computed tomography coronary angiography guided management will reduce the future risk of coronary heart disease death or non-fatal myocardial infarction compared to management guided by the current standard of care, a cardiovascular risk score.

NCT ID: NCT03910400 Recruiting - Clinical trials for ST Segment Elevation Myocardial Infarction

Early Assessment of QFR in STEMI-II

EARLYmyoQFR-II
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The study intends to provide new data on whether the noval method using quantitative flow ratio could assess microvascular dysfunction based on the previous study EARLY-MYO-QFR-I.

NCT ID: NCT03908463 Recruiting - Clinical trials for Coronary Artery Disease

KOMATE Registry: Korean Multicenter Angioplasty Team

Start date: October 5, 2018
Phase:
Study type: Observational

The investigators will enroll the patients who underwent PCI and was based on real world clinical practice to collect the data regarding demographic, clinical, procedural information and clinical outcome using case report forms.

NCT ID: NCT03891277 Recruiting - Iron-deficiency Clinical Trials

Efficacy and Safety of Ferrous Iron on the Prevention of Vascular Cognitive Impairment Among Patients With Cerebral Infarction/TIA (FAVORITE)

FAVORITE
Start date: April 1, 2019
Phase: Phase 2
Study type: Interventional

The prevalence of Vascular Cognitive Impairment(VCI) is high in patients after ischemic stroke or transient ischemic attack(TIA) . Effective therapy for the prevention of VCI remains limited. The primary purpose of this study is to evaluate the efficacy and safety of Ferrous iron versus placebo on the prevention of vascular cognitive impairment among patients with ischemic stroke/TIA complicated with Hemoglobin deficiency.

NCT ID: NCT03886675 Recruiting - Stroke Clinical Trials

Intervention With Cerebral Embolic Protection in TEVAR: Gaseous Protection

INTERCEPT:GP
Start date: November 14, 2022
Phase: N/A
Study type: Interventional

Vascular brain infarction (VBI) occurs in 67% of patients undergoing TEVAR. Overt stroke occurs in 13% of these patients and 88% of patients suffer from neurocognitive impairment. Cerebral air embolisation during the stent-graft deployment phase of TEVAR may be a cause of VBI. Standard treatment to de-air stent-grafts is through the use of a saline flush. This study aims to investigate whether carbon-dioxide or saline is the better fluid to de-air TEVAR stent-grafts prior to insertion in to the patient and compare VBI rate in the carbon-dioxide group and saline group.