drugset / Trial / NCT07138508

Oral Nicorandil for Prevention of No Reflow Phenomenon in Anterior STEMI Patients Undergoing PPCI

NCT07138508

RandomizedParallel-groupSingle-blindPrevention

Summary

Aim of the study is to Investigate the potential role of oral nicorandil in preventing the No reflow phenomenon in anterior ST-segment elevation myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PPCI). Assess whether nicorandil, a potassium channel activator, can effectively enhance myocardial perfusion in this specific clinical context. * In a randomized controlled trial study * All recruited patients were randomized to either the treatment or control group in a ratio of 1:1 using a computer-generated randomization sequence in relation to the order of participation in the study. Patients fulfilling the inclusion criteria and consenting to participate in the study were recruited.

Timeline

Start
2024-03-10
Primary completion
2025-02-28
Completion
2025-03-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nicorandil Other / unclassified 20 mg Oral