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NCT04665648CompletedPhase 4

Clinical Efficacy and sAfety of Intravenous Infusion of Nicorandil During Primary Percutaneous Coronary Intervention

Impact of Intravenous Administration of Nicorandil as Adjuncts to Reperfusion Treatment for Acute ST Segment Elevation Myocardial Infarction: a Multi-center Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 11 Mar 2025

Brief summary (registry, in English)

The investigators evaluate the efficacy and safety of intravenous administration of nicorandil as adjuncts to reperfusion treatment in acute ST-segment elevation acute myocardial infarction (STEMI) patients undergoing primary percutaneous coronary intervention (PCI).

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
1500 (actual)
First submitted
2 Dec 2020
Start date
1 Jun 2021
Primary completion date
31 Dec 2024
Lead sponsor
Fudan University
NCT number
NCT04665648

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 1500
  • From 1 Jun 2021 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • cardiac shock;
  • history of myocardial infarction or percutaneous coronary intervention or coronary artery bypass grafting (\<6 month);
  • history of the treatment of nicorandil (\<6 month);
  • history of intravenous nitrates before percutaneous coronary intervention;

Other

  • systolic blood pressure\<100mmHg;
  • aortic dissection;
  • contraindicated or intolerable to nicorandil;
  • pregnant or lactation period;
  • patients with an estimated survival time of less than 1 year.

Who the study is looking for

  • 18-80 years;
  • acute ST-segment elevation myocardial infarction within 12 hours of symptom onset;

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Zhongshan Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.