Major Adverse Cardiovascular Events (MACE)

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Review clinical trials related to Major Adverse Cardiovascular Events (MACE). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Prediction of Myocardial Injury After Non-Cardiac Surgery in Urologic Cancer Patients

This prospective multicenter observational study aims to evaluate the predictive value of artificial intelligence-based analysis of preoperative 12-lead electrocardiography for myocardial injury after non-cardiac surgery (MINS) and major adverse cardiovascular events (MACE) within 30 days after surgery in patients undergoing non-cardiac surgery for urologic cancer.

Participants needed: 200
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Korea University Anam HospitalUpdated: Jun 15, 2026
Eligibility criteria

Age ≥ 60 years [+5]

History of major adverse cardiovascular events (MACE) within 6 months prior to s... [+3]

Status: Recruiting

Serial Coronary CTA-based Plaque Progression Detection for Management of Coronary Heart Disease

The primary objective of this study is to evaluate whether a management strategy based on coronary computed tomography angiography (CCTA) for patients with non-obstructive coronary artery disease can improve the LDL-C target achievement rate compared to a traditional management strategy without follow-up CCTA, thereby reducing the incidence of major adverse cardiovascular and cerebrovascular events over a 3 years period, including all-cause mortality, myocardial infarction, ischemia driven revascularation and stroke.

Participants needed: 3,100
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Zhang longjiang,MDUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Age between 18 and 80 years old; [+2]

Patients who have experienced ACS or PCI/CABG; [+5]

Status: Not yet recruiting

Vitamin B Supplementation for Patients Undergoing Cardiovascular Surgery

This study is a multicenter, randomized controlled, double-blind, placebo-controlled parallel trial designed to evaluate the effect of perioperative supplementation with Compound Vitamin B on patients undergoing cardiovascular surgery. A total of 1,000 patients aged 18-80 years who are scheduled to receive cardiovascular surgeries such as coronary artery bypass grafting (CABG) and valve replacement will be enrolled. They will be randomly assigned at a 1:1 ratio to either the experimental group (perioperative supplementation with Compound Vitamin B tablets, once daily from 3 days before surgery to 6 months after surgery) or the control group (oral placebo), with both groups receiving standardized perioperative treatment.

Participants needed: 1,000
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Nanjing Medical UniversityUpdated: Jan 16, 2026Locations: 2
Eligibility criteria

Aged 18-80 years, regardless of gender; [+3]

Regular supplementation with Compound Vitamin B (daily dose ≥ 1.5 times the reco... [+6]