Unstable Angina (UA)

4

Review clinical trials related to Unstable Angina (UA). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Diagnostic Performance of Artificial Intelligence Algorithms in Prediction of Acute Coronary Syndrome Based on White Blood Cell Properties

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 (EC) and/or thrombocyte (TC) data, where available, improve or complement WBC-based AI prediction of ACS? * How does the diagnostic performance of the AI algorithms compare with high-sensitivity cardiac troponin (hs-cTn), and can the combination of AI algorithms and hs-cTn improve diagnostic performance? Participants will undergo clinical assessment and blood testing as part of usual clinical care. Their previously generated clinical information, hematology data, and hs-cTn results will be used to train and test the AI algorithms. Participation in the study does not determine the indication for coronary angiography or treatment, and no additional study-specific treatments are performed.

Participants needed: 3,350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: RobotDreams GmbHUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Male or female, aged 18 years or above. [+25]

Age below 18 years. [+4]

Status: Recruiting

Oregano and Basil Leaves and Coronary Artery Disease

The present study will examine the effects of increasing dietary polyphenol intake by consumption of oregano and basil leaves, on plasma inflammatory and lipid factors and total urinary polyphenol levels in patients who have recently had unstable angina.

Participants needed: 70
Trial details
Age: 30-75Biological sex: AllType: InterventionalSponsor: Shahid Beheshti University of Medical SciencesUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Patients diagnosed with unstable angina

Patients diagnosed with STEMI [+4]

Status: Recruiting

Breaking Fasts Ahead of Cardiac Caths

The goal of this clinical trial is to find out whether fasting is necessary before urgent inpatient cardiac catheterizations. For patients presenting with urgent heart-related pain or even mild heart attacks, researchers want to know whether eating and drinking before their procedure improves comfort without raising the risk of complications. The study will answer: * Does eating and drinking before the procedure improve patient comfort? * Does it increase the risk of adverse events like vomiting, aspiration (food or liquid entering the lungs), breathing problems, or death, etc? Participants will be randomly assigned to either: * A standard fasting group (no food for 6 hours, no clear liquids for 2 hours), or * A no-fasting group (able to eat and drink as usual). Patients will complete brief surveys before the procedure to assess comfort and satisfaction. Researchers will also review medical records weekly and 30 days later to monitor for safety outcomes.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of South FloridaUpdated: Dec 16, 2025Locations: 1
Eligibility criteria

All scheduled urgent inpatient non-high risk cardiac catheterizations for worsen...

High risk NSTEMI's defined as NSTEMI's with a GRACE score >140 points [+12]

Status: Not yet recruiting

Scientific Rationale and Design for a Prospective Study to Codify Coronary Lesions Based on Fluid Mechanics and Acoustic Mechanisms

From January 2020 to June 2025, patients coming to the cardiac catheterization laboratories (CCL) for out-patient coronary angiography with diagnosis of unstable angina were screened for inclusion. Patients were included in the study if they had previously undergone one or more coronary angiograms, allowing for a longitudinal comparison of dynamic flow and phenomena between the two or more angiograms.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: Tan Tao University, School of MedicineUpdated: Apr 17, 2025Duration: 3 Months
Eligibility criteria

Not listed