drugset / Trial / NCT06187727

Henagliflozin Reducing Infarct Size After Priamry PCI in Patients With ST Segment Elevation Myocardial Infarction

NCT06187727

Phase 4 Completed 248 enrolled Qian geng
RandomizedParallel-groupDouble-blindTreatment

Summary

This Randomized controlled intervention study recruited patients diagnosed with ST-segment elevation myocardial infarction (STEMI). A total of 240 patients were enrolled in either Henagliflozin group or control group. Patients in Henggliflozin group will be given by oral administration of Henggliflozin for 6 months post acute myocardial infarction. Prior to procedure, dynamic changes in myocardial enzymes were monitored. Major cardiovascular events, including non-fatal myocardial infarction, all-cause death, revascularization due to angina, and hospitalization for acute heart failure. This study aims to assess the impact of Henggelizin intervention on the reduction of myocardial infarction size (evaluated by cardiac enzyme) and improvement of left ventricular remodeling in patients with ST-segment elevation myocardial infarction.

Timeline

Start
2023-07-01
Primary completion
2025-01-01
Completion
2025-10-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Henagliflozin Small molecule Oral