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Infarction clinical trials

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NCT ID: NCT03370939 Completed - Clinical trials for Intracranial Artery Occlusion With Infarction (Disorder)

Endovascular Treatment Key Technique and Emergency Work Flow Improvement of Acute Ischemic Stroke

ANGEL-ACT
Start date: November 11, 2017
Phase:
Study type: Observational [Patient Registry]

Endovascular thrombectomy (EVT) is effective and safe for acute ischemic stroke (AIS) caused by large vessel occlusion (LVO) in major clinical trials. Whether the benefit of EVT in randomized trials could be generalized to clinical practice, especially in developing countries, remains unknown. The prospective Chinese ANGEL-ACT Registry (Endovascular Treatment Key Technique and Emergency Work Flow Improvement of Acute Ischemic Stroke) was established to evaluate the utilization, and subsequent outcomes of EVT treated AIS patients. This study is a multi-center, prospective registry study initiated by researchers, funded by National Key R&D Program of China. A total of 2,000 patients with acute ischemic stroke will undergo endovascular treatment. The hypothesis was that favorable outcomes from clinical trials could be achieved in clinical practice in China.

NCT ID: NCT03365492 Completed - Clinical trials for Coronary Artery Disease

BioFreedom Pharmacokinetic Study

Start date: March 12, 2018
Phase: N/A
Study type: Interventional

The purpose of this pharmacokinetic (PK) study is to characterize the maximum concentration (Cmax) and time-to-maximum concentration (Tmax) of Biolimus A9TM and its active metabolites sirolimus and everolimus in a cohort of coronary artery disease (CAD) patients following implantation of BioFreedomTM SS stent.

NCT ID: NCT03364387 Completed - Atrial Fibrillation Clinical Trials

Myocardial Infarction With Non-obstructive Coronary Arteries in Turkish Population

MINOCA-TR
Start date: March 5, 2018
Phase:
Study type: Observational

The objective of this study is to analyze the Demographics, Clinical Profiles, Management, in-Hospital and Long-Term Outcomes of Patients with Acute Coronary Syndrome Syndrome And Myocardial Infarction with Non-obstructive Coronary Artery Disease.

NCT ID: NCT03363035 Completed - Clinical trials for Myocardial Infarction

Safety and Efficacy of LMWH Versus Rivaroxaban in Chinese Patients Hospitalized With Acute Coronary Syndrome

H-REPLACE
Start date: January 15, 2018
Phase: Phase 4
Study type: Interventional

H-REPLACE trial is a prospective, randomized, open-label, active-controlled, multicenter study in participants with ACS (STEMI or NSTEMI, unstable angina). All eligible participants receiving background treatment of aspirin plus clopidogrel or ticagrelor will be randomly assigned to either oral rivaroxaban 2.5 mg twice daily or rivaroxaban 5 mg twice daily or subcutaneous (SC) enoxaparin 1mg/kg twice daily until hospital discharge or 12 hours before revascularization therapy for a maximum of 8 days.

NCT ID: NCT03358810 Completed - Clinical trials for Dysphagia Following Cerebral Infarction

Pharyngeal Electrical Stimulation Evaluation for Dysphagia After Stroke

PhEED
Start date: March 31, 2018
Phase: N/A
Study type: Interventional

This is a randomized, sham-controlled, patient masked, outcome assessor-blinded study to assess a Pharyngeal Electrical Stimulation (PES) Catheter for treatment of oropharyngeal dysphagia following a stroke.

NCT ID: NCT03358368 Completed - Clinical trials for Myocardial Infarction

MCG Post Myocardial Infarction Study

Start date: March 22, 2018
Phase:
Study type: Observational

The study is being performed to evaluate a new portable medical device, the Creavo Vitalscan Magnetocardiograph (Vitalscan) on patients who have had a confirmed myocardial infarction (heart attack) within the previous 12 weeks.

NCT ID: NCT03350971 Completed - Clinical trials for Myocardial Infarction

Influence of Virtual Reality on Myocardial Revascularization

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

Coronary artery disease is a dysfunction characterized by the narrowing of the coronary arteries in due to the accumulation of atheromatous plaques. The surgery of myocardial revascularization is a surgical procedure of choice performed in individuals with to improve symptoms and survival. Cardiovascular surgeries of this size in an extended time of rest after the procedure. Such immobility may have repercussions to the functionality of the individual. Thus, the early mobilization with the use of reality in the Intensive Care Units (ICU) emerges as a potential means of of complications in the postoperative period of cardiac surgery.

NCT ID: NCT03350568 Completed - Osteoarthritis Clinical Trials

Dietary Antioxidants and Chronic Diseases-The Swedish National March Cohort

Start date: October 1, 1997
Phase: N/A
Study type: Observational

Dietary antioxidants might protect from the development of chronic diseases by reducing levels of oxidative stress. The investigators therefore investigated the effect of dietary Non Enzymatic Antioxidant Capacity, which measures interactions between antioxidants in the whole diet, on the risk of 1) myocardial infarction and 2) osteoarthritis.

NCT ID: NCT03342521 Completed - Clinical trials for Myocardial Infarction

OFDI-Quantified Intracoronary Thrombus, Antiplatelet Pretreatment Effect and Myocardial Reperfusion

ODIPP
Start date: October 13, 2017
Phase:
Study type: Observational

The management of ST-elevation myocardial infarction in the acute phase requires an optimal antiaggregation combining aspirin and a P2Y12 inhibitor (clopidogrel, prasugrel or ticagrelor). Primary percutaneous coronary intervention must be performed within 2 hours of first medical contact. However, even with the new P2Y12 inhibitors, effective platelet inhibition which is required to inhibit the progression of intracoronary thrombus, is present only in half of the patients at 2 hours. Optical coherence tomography (OCT) is the reference method for visualizing and quantifying intracoronary thrombus. The post-stenting intracoronary residual mass evaluated in OCT was associated with altered myocardial reperfusion indices, which were themselves associated with the prognosis of the patient. However, the determinants of this post-stenting residual mass -mostly thrombotic- remain unknown. Measurement of platelet reactivity (expressed as P2Y12 Reaction Unit and Aspirin Reaction Unit) by simple turbidimetric tests (VerifyNow) is available in the cathlab. Enhanced platelet reactivity is reported in patients with acute coronary syndrome and represents a high-risk situation for recurrent coronary events in this setting. The study aims to: 1. to evaluate the relationship between the post-stenting residual intracoronary mass evaluated in OCT and the platelet response at the time of the PCI evaluated by Verify Now 2. to confirm the impact of the residual mass measured by OCT on the EKG and angiographic myocardial reperfusion indices 3. identify patients with high thrombotic risk who may require more intensive antithrombotic therapy 4. identify simple biological markers associated with the residual mass measured by OCT

NCT ID: NCT03340948 Completed - Clinical trials for Coronary Artery Disease

The Mindfulness Intervention as Myocardial Infarction Rehabilitation Additive (MIMIRA) Study

MIMIRA
Start date: January 31, 2012
Phase: N/A
Study type: Interventional

The Mindfulness Intervention as Myocardial Infarction Rehabilitation Additive (MIMIRA) study aimed at studying the feasibility and acceptability of Mindfulness Based Stress Reduction - an 8 week course in meditation and yoga - in patients with a recent coronary artery event and elevated depressive symptoms. To address these questions patients with elevated scores on a depression scale were invited to participate in MBSR, and there evaluation of the course as well as a panel of psychological risk factors and resources was measured.