Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Heart Attack from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 19
- Active, not recruiting: 5
- Completed: 12
- Other: 14
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT06252168 — Registry of Acute Myocardial Infarction
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
| Enrollment | 97500 |
| Study Type | OBSERVATIONAL |
| Conditions | Myocardial Infarction, Acute |
The Registry of Acute Myocardial Infarction (RAMI) aims at regular and centralized acquiring and processing standard information about verified and suspected cases of acute myocardial infarction (AMI), monitoring of AMI cases, and establishing AMI diagnosis based on standard diagnostic criteria by doctors involved in the registry. The RAMI obtains data from all medical institutions, which could…
NCT04416581 — Potassium-Competitive Acid Blocker Versus pROton-Pump Inhibitor for GastroproTECTion Strategies In Patients at High Gastro-Intestinal Bleeding Risk Receiving Antithrombotic Therapy
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Duk-Woo Park, MD |
| Enrollment | 3320 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Artery Disease; Percutaneous Coronary Intervention; Acute Coronary Syndrome; Myocardial Infarction |
| Interventions | ; |
The primary aim of this study is to evaluate the efficacy and safety of novel P-CAB (tegoprazan 50 mg once daily) as compared with standard PPI (rabeprazole 20 mg once daily) for protection of GI events in patients with known cardiac and vascular disease receiving chronic use of antithrombotic drugs (either antiplatelets, OAC, and its combinations) who are at high GI bleeding risk. The primary …
NCT04968808 — Timing of FFR-guided PCI for Non-IRA in NSTEMI and MVD (OPTION-NSTEMI)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Chonnam National University Hospital |
| Enrollment | 1014 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction, Acute; Multi-Vessel Coronary Artery Stenosis; Multi Vessel Coronary Artery Disease |
| Interventions | ; |
Many patients with non-ST-segment elevation myocardial infarction (NSTEMI) have multivessel coronary artery disease (MVD), which is associated with poor clinical outcomes. However, there have been few studies regarding revascularization strategy in patients with NSTEMI and MVD. Therefore, we planned to perform prospective, open-label, randomized trial to evaluate the efficacy and safety of imme…
NCT05491200 — Comparison Of Reduced DAPT Followed by P2Y12 Inhibitor Monotherapy With Prasugrel vs stAndard Regimen in STEMI Patients
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Research Maatschap Cardiologen Rotterdam Zuid |
| Enrollment | 1656 |
| Study Type | INTERVENTIONAL |
| Conditions | ST Elevated Myocardial Infarction; Dual Antiplatelet Therapy |
| Interventions | ; ; |
The study is a multi-centre, Open-label, Randomized Controlled, 1:1 trial comparing Prasugrel-based short DAPT (30-45 days) followed by Prasugrel monotherapy versus standard DAPT regimen in STEMI patients in terms of safety and efficacy endpoints.
In the subgroup of STEMI patients with MVD, a sub-randomization will allow a comparison between a complete revascularization OCT-guided versus compl…
NCT06295679 — A Study Assessing Repatha® in Combination With Standard of Care (SOC) Compared With SOC on Major Cardiovascular Events in Chinese Participants With Atherosclerotic Cardiovascular Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Amgen |
| Enrollment | 7000 |
| Study Type | OBSERVATIONAL |
| Conditions | Major Cardiovascular Event; Established Atherosclerotic Cardiovascular Disease |
The primary objective of the study is to evaluate real-world effectiveness of treatment with Repatha® in combination with SOC, compared with SOC alone, on the risk for cardiovascular (CV) death, myocardial infarction (MI), stroke, hospitalization for unstable angina, or coronary revascularization, whichever occurs first, in participants with established atherosclerotic CV disease (ASCVD) treate…
NCT05699005 — Individualized or Conventional Transfusion Strategies During Peripheral VA-ECMO
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | University Hospital, Lille |
| Enrollment | 236 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiogenic Shock; Extracorporeal Membrane Oxygenation; Transfusion Related Complication; Anemia; Oxygen Delivery |
| Interventions |
This multicenter randomized controlled trial compare two transfusion strategies of red blood cells transfusion in patients supported by veno-arterial extracorporeal membrane oxygenation for refractory cardiogenic shock.
An individualized transfusion strategy based on ScVO2 level, is compared to a conventionnal strategy based on predefined hemoglobin threshold. The primary endpoint is the consu…
NCT06384846 — Diagnostic Performance of Artificial Intelligence Algorithms in Prediction of Acute Coronary Syndrome Based on White Blood Cell Properties
| Status | Recruiting |
| Phase | N/A |
| Sponsor | RobotDreams GmbH |
| Enrollment | 3350 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Coronary Syndrome; Angina Pectoris; NSTEMI - Non-ST Segment Elevation MI; STEMI - ST Elevation Myocardial Infarction; Unstable Angina (UA) |
The goal of this observational study is to evaluate whether artificial intelligence (AI) algorithms can predict or exclude acute coronary syndrome (ACS) in adults using data generated by routine hematology testing. The main questions the study aims to answer are:
- Can AI algorithms based on white blood cell (WBC) data predict or exclude ACS in subjects with suspected ACS?
- Can erythrocyte (E…
NCT06964685 — Assessment of Support With Impella® Best Practices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Abiomed Inc. |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | AMI Cardiogenic Shock |
| Interventions |
The observational study titled “Observational Assessment of Support with Impella Best Practices in Acute Myocardial Infarction Complicated by Cardiogenic Shock (OASIS-AMICS)” aims to evaluate the safety outcomes of patients with acute myocardial infarction complicated by cardiogenic shock (AMICS) who receive Impella CP during percutaneous coronary intervention (PCI) and who are managed with Imp…
NCT07136012 — OCEAN(a)-PreEvent - Olpasiran Trials of Cardiovascular Events And LipoproteiN(a) Reduction to Prevent First Major Cardiovascular Events
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Amgen |
| Enrollment | 11000 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiovascular Disease |
| Interventions | ; |
The primary objective is to evaluate the effect of olpasiran, compared to placebo, on the risk for coronary heart disease death (CHD death), myocardial infarction, or urgent coronary revascularization in participants at risk for a first major cardiovascular event with elevated lipoprotein(a) (Lp[a]).
NCT07102628 — Evaluation of Efficacy and Safety of Early in Hospital Initiation of Inclisiran Treatment in Patients With Acute Coronary Syndromes
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Coronary Syndrome |
| Interventions | ; |
The purpose of this trial is to learn about the effects of inclisiran in people with serious heart conditions (acute coronary syndromes), when this treatment is started early after hospital admission. To do this, researchers will test the effects of inclisiran compared to placebo, when given with standard treatment.
NCT07252856 — Transcultural Digital Solutions in Phase III Cardiac Rehabilitation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fondazione Don Carlo Gnocchi Onlus |
| Enrollment | 306 |
| Study Type | INTERVENTIONAL |
| Conditions | Heart Failure; Myocardial Infarction |
| Interventions |
Multicenter Prospective Controlled Randomized Trial, open-label, in patients with atherosclerotic cardiovascular disease (ASCVD) (acute coronary syndrome or chronic coronary syndrome and ischemic heart failure) and an approved indication for cardiac rehabilitation (CR). Patients completing phase II CR will be randomized 1:1 to usual Phase-III care (standard care) versus standard care plus the D…
NCT07655479 — Rapid Microaxial Flow Pump Support and Escalation in Patients With Myocardial Infarction Associated Cardiogenic Shock and Persistent Need of Hemodynamic Support
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital of Cologne |
| Enrollment | 115 |
| Study Type | OBSERVATIONAL |
| Conditions | Cardiogenic Shock Post Myocardial Infarction |
| Interventions |
The aim of this trial is to evaluate whether a structured and time-optimized escalation strategy from a transfemoral microaxial flow-pump (Impella CP™) to the Impella 5.5™ microaxial flow-pump is associated with improved clinical outcomes and fewer adverse events in patients with cardiogenic shock due to acute myocardial infarction
NCT07517263 — An Open Label Extension (OLE) Study (Following Completion of CTQJ230A12301) to Evaluate Long-term Safety and Tolerability of Pelacarsen (TQJ230)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 5700 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiovascular Disease and Lipoprotein(a) |
| Interventions |
This open-label extension study will provide post-trial access to pelacarsen (TQJ230) to participants who have successfully completed the double-blind parent study (CTQJ230A12301).
NCT07428473 — A Study of STX-1150 in Participants With Elevated Low-Density Lipoprotein Cholesterol (LDL-C)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Monash University |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Elevated LDL-C and High Cholesterol |
| Interventions |
STX-1150 is an investigational therapy designed to lower LDL-C by silencing a gene called PCSK9 in the liver. STX-1150 does not edit or permanently change the gene. STX-1150 comprises an mRNA and guide RNA (gRNA) delivered via lipid nanoparticles (LNP) for intravenous infusion. The mRNA produces a protein that switches off the PCSK9 gene expression without altering the DNA sequence. This proces…
NCT07619885 — The Pharmacokinetics and Pharmacodynamics Study of Evategrel CG-0255 Besylate)and Plavix® in Healthy Participants
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Shanghai CureGene Pharmaceutical Co., Ltd. |
| Enrollment | 136 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Coronary Syndromes (ACS); Recent Myocardial Infarction; Recent Stroke; Peripheral Arterial Disease |
| Interventions | ; ; |
CG-0255 is a novel investigational prodrug of the active metabolite of Plavix®, but with different active metabolite conversion routes. This is a randomized, open-label and Plavix®-controlled study to compare the PK and PD of CG-0255 Besylate and Plavix® in healthy participants.
NCT07626060 — Diagnostic Accuracy of GPT-4o and Claude for HEART Score Calculation in Chest Pain
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Marmara University Pendik Training and Research Hospital |
| Enrollment | 690 |
| Study Type | OBSERVATIONAL |
| Conditions | Emergency Medicine; Artificial Intelligence (AI); Artificial Intelligence (AI) in Diagnosis; Chest Pain Rule Out Myocardial Infarction |
| Interventions | ; ; |
This prospective observational diagnostic accuracy study evaluates whether large language models (LLMs) - GPT-4o (OpenAI, gpt-4o-2024-11-20) and Claude (Anthropic, claude-sonnet-4-6) - can accurately calculate HEART scores from unstructured Turkish clinical notes and predict 30-day major adverse cardiac events (MACE) in emergency department patients presenting with non-traumatic chest pain.
Th…
NCT07636642 — Sixth Generation High-sensitivity Cardiac Troponin T for the Early Rule Out of Myocardial Infarction: a Controlled Before and After Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Edinburgh |
| Enrollment | 19500 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction |
| Interventions | ; |
Cardiac troponin is a protein released into the blood when the heart muscle is damaged. Measuring this protein helps doctors diagnose a heart attack (also called a myocardial infarction). Modern blood tests, known as high-sensitivity cardiac troponin assays, can detect very small amounts of this protein.
A new version of this test, called Troponin T high-sensitivity Gen 6, has recently been de…
NCT07467213 — Routine Use of Potassium Competitive Acid Blocker vs. Guideline-Directed Gastrointestinal Protection Strategy in Acute Myocardial Infarction
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Samsung Medical Center |
| Enrollment | 5000 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myocardial Infarction (AMI); Gastrointestinal Bleeding |
| Interventions | ; |
This study aims to compare the clinical outcomes between routine use of potassium competitive acid blocker (P-CAB) and guideline-directed gastrointestinal (GI) protection strategy in patients with acute myocardial infarction (AMI) undergoing percutaneous coronary intervention (PCI) and being treated with dual antiplatelet therapy (DAPT).
NCT07362446 — Prevention of Reperfusion Injury Outcomes Through Effective Cardioprotection Targeting Myocardial Infarction
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Nyrada Pty Ltd |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction; Reperfusion Injury; AMI; STEMI (ST Elevation MI) |
| Interventions | ; |
This study is open to adults with ST elevation myocardial infarction (heart attack) undergoing primary percutaneous coronary intervention (PCI). The purpose of this study is to determine whether a medicine called Xolatryp is safe and effective in improving cardiac outcomes. One dose of Xolatryp will be tested in this study.
Participants are put into two groups randomly, which means by chance. …
Active, Not Recruiting
NCT00590200 — GeneBank at the Cleveland Clinic: Molecular Determinants of Coronary Artery Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | The Cleveland Clinic |
| Enrollment | 9880 |
| Study Type | OBSERVATIONAL |
| Conditions | Cardiovascular Diseases |
This proposal delineates a research plan to collect blood from patients undergoing heart catheterization or who have had a heart catheterization within one year and are coming in for outpatient appointments, or who have scheduled cardiac CT scans at the Cleveland Clinic over a five-year period for the purpose of establishing a gene bank registry. In addition, the University of North Carolina at…
NCT04626882 — Timing of FFR-guided PCI for Non-IRA in STEMI and MVD (OPTION-STEMI)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Chonnam National University Hospital |
| Enrollment | 994 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction, Acute; Multi-Vessel Coronary Artery Stenosis |
| Interventions |
Patients with STEMI (ST-segment elevation myocardial infarction) with multivessel disease which have PCI (percutaneous coronary intervention)-suitable non-IRA (infarct related artery) will be randomized to immediate complete revascularization group or staged revascularization group by 1:1 fashion. Non-IRA lesion which have equal or more than 70% diameter stenosis by visual estimation will be re…
NCT04260958 — Remote Exercise SWEDEHEART Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sahlgrenska University Hospital |
| Enrollment | 1500 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction |
| Interventions |
The overall aim of the study is to evaluate if remote video exercise-based cardiac rehabilitation (exCR), offered as an alternative to centre-based exCR, can increase participation in exCR sessions post myocardial infarction (MI).
NCT05739383 — A Study of Inclisiran to Prevent Cardiovascular Events in High-risk Primary Prevention Patients.
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 14012 |
| Study Type | INTERVENTIONAL |
| Conditions | Primary Prevention of Atherosclerotic Cardiovascular Disease |
| Interventions | ; |
CKJX839D12302 is a pivotal Phase III study designed to test the hypothesis that treatment with inclisiran sodium 300 milligram (mg) subcutaneous (s.c.) administered on Day 1, Day 90, and every 6 months thereafter in patients at high cardiovascular (CV) risk without a prior major atherosclerotic cardiovascular disease (ASCVD) event will significantly reduce the risk of 4-Point-Major Adverse Card…
NCT06853626 — One-hoUr Troponin Using a High-sensitivity Point-Of-Care Assay in Emergency Primary Care
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Oslo |
| Enrollment | 2500 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myocardial Infarction (AMI); Chest Pain; Acute Coronary Syndromes (ACS); Non-cardiac Chest Pain; Troponin |
| Interventions |
Acute chest pain is a prevalent medical emergency in primary emergency care settings. Triage of chest pain prior to hospital admission presents significant challenges due to the absence of sufficiently sensitive diagnostic tools. Clinical signs, symptoms, risk assessment scores, or a normal electrocardiogram (ECG) can reliably exclude acute myocardial infarction (MI). This diagnostic uncertaint…
Not Yet Recruiting
NCT07646977 — CORonary Thrombus Modification to Prevent MIcrovascular Damage in Patients With ST-segment Elevation Myocardial Infarction (The CORMI Trial)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Odense University Hospital |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | ST Elevation Myocardial Infarction; Coronary Microvascular Dysfunction; Percutaneous Coronary Intervention |
| Interventions | ; |
The aim of this study is to evaluate the effects of coronary thrombus modification on preventing the microvascular damage associated with primary percutaneous coronary intervention (PCI), and to limit the associated myocardial damage assessed by myocardial salvage index after 3 months. Furthermore, the project will evaluate coronary microvascular damage assessed invasively using both continuous…
NCT07684924 — Early Ga-68 FAPI PET/MR After Acute Myocardial Infarction
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ankara University |
| Enrollment | 25 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Myocardial Infarction (AMI) |
| Interventions |
Acute myocardial infarction (AMI) initiates a complex myocardial repair process involving inflammation, fibroblast activation, and extracellular matrix remodeling, which may ultimately lead to adverse left ventricular remodeling and impaired cardiac function. Fibroblast activation protein (FAP)-targeted positron emission tomography (PET) enables noninvasive visualization of activated fibroblast…
NCT07689591 — Noninvasive Artificial Venous Stasis for Reperfusion in STEMI
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Firat University |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | STEMI - ST Elevation Myocardial Infarction |
This prospective, randomized study was designed to evaluate whether the noninvasive artificial venous stasis / RE-START procedure, administered prior to primary percutaneous coronary intervention, increases the frequency of spontaneous coronary reperfusion in the infarct-related artery.
NCT07687576 — Comparative Evaluation of Sustained meChanical AsPiration Thrombectomy and no Thrombus Modification for Pre-stent Thrombus bUrden Reduction in Patients With Acute Myocardial Infarction Study: the CAPTURE AMI Study
| Status | Not yet recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Oxford University Hospitals NHS Trust |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | STEMI - ST Elevation Myocardial Infarction |
| Interventions | ; |
The CAPTURE AMI trial is an investigator-initiated, single-centre, two-arm, randomised controlled trial. Patients aged ≥ 18 years who present with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI) will be enrolled after angiographic evidence of a high thrombus burden (TIMI thrombus grade ≥ 4) and meeting the inclusion criteria laid out in se…
NCT07684742 — Early Single Antiplatelet Therapy After IVUS-Guided PCI in Acute Coronary Syndrome
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Gyeongsang National University Hospital |
| Enrollment | 1900 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Coronary Syndromes; STEMI; NSTEMI; Unstable Angina |
| Interventions | ; |
This is a prospective, open-label, multicenter, randomized, phase IV clinical trial designed to evaluate the safety and efficacy of early aspirin discontinuation followed by potent P2Y12 inhibitor monotherapy after intravascular ultrasound (IVUS)-guided drug-eluting stent implantation in patients with acute coronary syndrome. A total of 1,900 patients who achieve complete revascularization afte…
NCT07621380 — Ertugliflozin’s Effect on Heart Function in Diabetic Patients After Myocardial Infarction
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Shanghai Zhongshan Hospital |
| Enrollment | 476 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus Myocardial Infarction |
| Interventions | ; |
This prospective, randomized, open-label, blinded endpoint (PROBE) trial evaluates the efficacy of early ertugliflozin initiation (10 mg daily) compared to standard care alone on cardiac function in 476 adult patients with type 2 diabetes mellitus (T2DM) following a first acute myocardial infarction (AMI). The study is supported by scientific rationale suggesting potential effects of ertugliflo…
NCT07656259 — COMPARE-VENT Feasibility Pilot Study
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Respiration Failure; Cardio Vascular Disease; Cardiogenic Pulmonary Oedema; Critical Illness; Mechanical Ventilation |
| Interventions | ; |
Cardiac disease complicated by respiratory insufficiency comprises the most frequent indication for cardiac intensive care unit (CICU) admission, with nearly one-third patients requiring advanced respiratory support and over 20% patients requiring invasive mechanical ventilation (IMV). IMV among patients with impaired cardiovascular reserve is further compounded by the adverse impact of positiv…
NCT07687017 — CRP Apheresis in Infarct-Related Cardiogenic Shock
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Leipzig Heart Science gGmbH |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiogenic Shock; Acute Myocardial Infarction (AMI) |
| Interventions | ; |
Cardiogenic shock complicating acute myocardial infarction remains associated with high short-term mortality despite guideline-directed therapy. Systemic inflammation, particularly elevated C-reactive protein (CRP), may contribute to ongoing myocardial injury and organ dysfunction.
The CRP-SHOCK trial is an investigator-initiated, prospective, randomized, open-label, multicenter pilot study ev…
NCT07663201 — Cardiovascular Risk in Patients With IBD
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | IRCCS Policlinico S. Donato |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Ulcerative Colitis (UC); Crohn’s Diseases; Cardiovascular Risk |
In this study our Research Hospital San Donato Policlinic ask your partipation with the aim to evaluate the risk of cardiovascular complication (i.e. stroke, myocardial infarction) in patients with inflammatory bowel disease. Multiple parameters (therapy, disease activity, life style) and investigations (DNA, stool, lab tests) will be evaluate with the support of artificial intelligence methodo…
NCT06904144 — Health Coaching for Patients With Cardiovascular Disease
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ohio State University |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Congestive Heart Failure Treated; Myocardial Infarction (MI); Coronary Artery Disease; Congestive Heart Failure Chronic |
| Interventions |
For patients discharged with a diagnosis of cardiovascular disease coronary artery disease resulting in myocardial infarction and/or congestive heart failure, this study will evaluate if the addition of 12 virtual health coaching sessions over the course of 16 weeks will improve physiological, psychological, and social health outcomes, prove acceptable and satisfactory for these patients with C…
Completed Trials
NCT03507270 — One-hour Diagnostic Algorithm for NSTEMI
| Status | Completed |
| Phase | N/A |
| Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Non ST Segment Elevation Myocardial Infarction |
| Interventions |
Predictable values of the 1-hour algorithm for estimating the concentration of troponin using highly sensitive reagents are 98-100% for excluding myocardial infarction (MI) and 75-80% for identifying this pathology. Such algorithms are developed for the rapid confirmation or exclusion of myocardial infarction without ST-segment elevation and, when combined with clinical data and electrocardiogr…
NCT03677466 — Intramyocardial Haemorrhage in Patients With Primary STEMI
| Status | Completed |
| Phase | N/A |
| Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction; STEMI; Myocardial Necrosis; Myocardial Injury |
| Interventions | ; |
The purpose of the study is to assess the frequency and intensity of intramyocardial haemorrhage in patients with primary STEMI and different reperfusion strategies.
NCT03872401 — Effect of Evolocumab in Patients at High Cardiovascular Risk Without Prior Myocardial Infarction or Stroke
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Amgen |
| Enrollment | 12301 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Heart Disease (CHD) |
| Interventions | ; |
This study will assess the effect of lowering low-density lipoprotein cholesterol (LDL-C) with evolocumab on major cardiovascular events in adults without a prior myocardial infarction (MI) or stroke who are at high risk of a cardiovascular event.
NCT04573751 — The EPIVER Randomized Controlled Trial
| Status | Completed |
| Phase | N/A |
| Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | ST Elevation Myocardial Infarction; Percutaneous Coronary Intervention; No-Reflow Phenomenon |
| Interventions | ; ; |
The trial aims to estimate the efficacy and safety of the intracoronary administration of adrenalin, verapamil, as well as their combination compared to standard treatment in patients with STEMI and refractory coronary no-reflow despite conventional treatment during percutaneous coronary intervention (PPCI)
NCT04765956 — Intravascular Identification and Drug-Eluting Balloon Treatment of Vulnerable Lipid-Rich Plaques
| Status | Completed |
| Phase | N/A |
| Sponsor | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Artery Disease |
| Interventions |
Rationale: Two-thirds of intracoronary thrombi causing acute coronary syndrome (ACS) result from rupture of lipid-rich plaques (LRP). After treatment of the culprit lesion in ACS patients, additional LRPs are found in approximately 50% of patients. Near infrared spectroscopy (NIRS) combined with intracoronary ultrasound (IVUS) can identify these vulnerable plaques during coronary angiography (C…
NCT06186102 — Polyamine Treatment in Elderly Patients With Coronary Artery Disease
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | University of Aarhus |
| Enrollment | 187 |
| Study Type | INTERVENTIONAL |
| Conditions | Ischemic Heart Disease; Myocardial Infarction; Cardiovascular Diseases; Hypertensive Heart Disease; Hypertension |
| Interventions | ; |
The present study is testing spermidine treatment in elderly patients with coronary artery disease. The study is a randomized, double-blind, placebo-controlled, two-armed, parallel-group, single centre, clinical study.
NCT06247358 — Frailty, Physical Capacity and Lung Function in Postoperative Cardiac Surgery Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Sao Paulo General Hospital |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Cardiac Infarct; Cardiac Valve Disease; Fragility; Physical Disability |
The goal of this observational and prospective study is to investigate changes in physical performance, lung function, and respiratory and peripheral muscle strength in patients during the postoperative period following coronary artery bypass grafting (CABG) and valve replacement surgery..
NCT06457815 — Iron Deficiency in Acute Myocardial Infarction: Prevalence Pilot Study
| Status | Completed |
| Phase | N/A |
| Sponsor | South Tees Hospitals NHS Foundation Trust |
| Enrollment | 70 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Myocardial Infarction |
Acute Myocardial Infarction (heart attacks) affect about 86000 people each year in the UK. Given this large number of people, it is important that health teams look at ways to ensure the best care to improve outcomes after a heart attack.
In related heart conditions, the role of iron is important, but there isn’t much information about what effect iron levels have on patients following a heart…
NCT05605288 — Distal Versus Conventional Transradial Artery Access for Coronary Catheterization in Patients With STEMI
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital of Patras |
| Enrollment | 554 |
| Study Type | INTERVENTIONAL |
| Conditions | ST Elevation Myocardial Infarction; Coronary Artery Disease; Distal Transradial Artery; Transradial Artery; Coronary Catheterization |
| Interventions |
Recently, a novel distal transradial, through anatomical snuffbox, approach has been proposed for undertaking percutaneous coronary angiography and interventions. The existing literature has evaluated distal transradial access (dTRA) as a feasible and safe approach, with faster hemostasis, lower rates of periprocedural complications and reduced incidence of radial artery occlusion (RAO). Aim of…
NCT06759259 — Mannitol Administration for Delerium Prevention
| Status | Completed |
| Phase | N/A |
| Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Myocardial Infarction (MI); Delirium, Intensive Care Unit, Randomised Controlled Trial |
The aim of the study is to evaluate the efficacy of adjuvant administration of mannitol for the prevention of delirium in patients with myocardial infarction.
NCT07676656 — Neck-to-Waist Ratio Identifies Chronic Hypertensive Phenotype and Occlusive Myocardial Infarction in Patients Presenting With Acute Coronary Syndrome
| Status | Completed |
| Phase | N/A |
| Sponsor | Ercis Sehit Rıdvan Cevik State Hospital |
| Enrollment | 238 |
| Study Type | OBSERVATIONAL |
| Conditions | Hypertension; Acute Coronary Syndrome (ACS) Undergoing Percutaneous Coronary Intervention (PCI); Obesity (Disorder) |
aim of this study was to evaluate the relationship between multiple conventional and novel anthropometric measurements and hypertension in patients presenting to the ED with ACS and whether anthropometric indices differ according to admission BP status and evaluated the relationship between regional adiposity-related anthropometric phenotypes and cardiovascular stress response in ACS presentati…
NCT06939738 — Artificial Intelligence Scalable Solution for ST Myocardial Infarction
| Status | Completed |
| Phase | N/A |
| Sponsor | Idoven 1903 S.L. |
| Enrollment | 489 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Myocardial Infarction (AMI) |
The ASSIST clinical study is an observational, multicenter study to assess the performance of a cloud-based and AI-powered electrocardiogram (ECG) analysis platform, named Willem™, developed to detect Acute Myocardial Infarction (AMI).
The main objectives are to compare Willem™ performance to detect and triage ECG patterns associated with AMI compared with human ECG interpretation, and to asse…
Other (Terminated)
NCT00546260 — Safety and Efficacy Study of Adjunctive Antiplatelet Therapy Prior to Primary PCI in Patients With STEMI
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | Alexion Pharmaceuticals, Inc. |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction |
| Interventions | ; |
Safety and efficacy of adjunctive antiplatelet therapy prior to primary percutaneous intervention (PCI) in patients with ST-Elevation Myocardial Infarction (STEMI)
NCT02789098 — Relationship Between Left Ventricular Remodeling, Coronary Endothelial Function and Myocardial Fibrosis Using Positron Emission Tomography in Patients With ST-elevation Myocardial Infarction
| Status | Terminated |
| Phase | N/A |
| Sponsor | University Hospital, Caen |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | ST Elevation Myocardial Infarction |
| Interventions |
Left ventricular remodeling is a common complication in patients with ST-elevation myocardial infarction (STEMI ) and may lead to heart failure. Hemodynamic, metabolic and inflammatory mechanisms are involved in this pathophysiological process. Recent data demonstrated that remote, noninfarct-related region of the myocardium is also implicated. There is no data about the assessment of coronary …
NCT05724576 — Intracoronary Administration of OmniMSC-AMI for Acute ST-segment Elevation Myocardial Infarction Patients
| Status | Terminated |
| Phase | Phase 1 |
| Sponsor | Taiwan Bio Therapeutics Inc. |
| Enrollment | 1 |
| Study Type | INTERVENTIONAL |
| Conditions | Safety Issues |
| Interventions |
This study will test the hypothesis intracoronary administration of OmniMSC-AMI (allogenic bone marrow-derived mesenchymal stem cells) just after finishing the primary percutaneous coronary intervention (PCI) in ST-segment elevation myocardial infarction (STEMI) patients without cardiogenic shock is safe and may provide benefit on improving left ventricular ejection fraction (LVEF) during clini…
NCT06139328 — IRI-EXPLORE: A Study to Test Whether BI 765845 Helps People Who Have Had a Heart Attack
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | Boehringer Ingelheim |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Myocardial Infarction |
| Interventions | ; |
This study is open to adults aged 18 and over who have just had a heart attack. The purpose of this study is to find out whether a medicine called BI 765845 helps people who have had a heart attack. The investigators also want to test how well different doses of BI 765845 work and how they are tolerated by people who have had a heart attack.
Participants are randomly assigned to receive either…