Oral Nicorandil in ST Elevation Myocardial Infarction Patients Undergoing Primary Percutaneous Coronary Intervention

Sponsor
Ahmed Abdel Nasser Abdel Rady (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04632121
Collaborator
(none)
300
32.9

Study Details

Study Description

Brief Summary

  • To study the effects of early oral administration of nicorandil in the setting of PPCI among STEMI patients on early angiographic, electrocardiographic, echocardiographic and hard clinical outcomes.

  • To assess the possible benefits of nicorandil on myocardial reperfusion through LGE- CMR substudy after 3 months.

Condition or Disease Intervention/Treatment Phase
  • Drug: Nicorandil 20 MG

Detailed Description

Nicorandil is a nicotinamide ester that dilates peripheral and coronary resistance vessels via action on ATP-sensitive potassium channels and possesses a nitrate moiety that promotes systemic venous and coronary vasodilation. As a result of these dual actions, nicorandil reduces preload and afterload and results in an increase in coronary blood flow. In addition to these effects, nicorandil may have cardioprotective actions mediated through the activation of potassium channel .

Previous study on the effect of nicorandil on patients with stable angina has shown significant improvement in outcome due to a reduction in major coronary events.

Acute occlusion of the coronary artery in the STEMI patient subjects the myocardium supplied by that vessel to acute myocardial ischemia, thereby demarcating the area at risk (AAR) of potential MI, should the acute coronary occlusion be sustained or permanent. If the period of acute myocardial ischemia is prolonged (more than 20 minutes) a "wave front" of cardiomyocyte death begins in the subendocardium and extends transmurally over time toward the epicardium.

The deprivation of oxygen and nutrient supply results in a series of abrupt biochemical and metabolic changes within the myocardium. The absence of oxygen halts oxidative phosphorylation, leading to mitochondrial membrane depolarization, ATP depletion, and inhibition of myocardial contractile function.

Ischemia-Reperfusion injury (IRI) is defined as the paradoxical exacerbation of cellular dysfunction and death, following restoration of blood flow to previously ischemic tissues. Reestablishment of blood flow is essential to salvage ischemic tissues. However reperfusion itself paradoxically causes further damage, threatening function and viability of the organ.

Early intra-coronary administration of nicorandil has been shown to reduce the damage in the myocardial microcirculation caused by PPCI and the myocardial infarct size in patients with AMI .

Nicorandil prior to reperfusion was suggested to improve coronary flow. Furthermore, suppression of ventricular arrhythmia, and improvement of left ventricular function were demonstrated in patients who suffered from AMI and underwent primary PCI. But the definite clinical benefits of nicorandil were not found, which may be due to the small sample size of the selected studies .

Compared with intracoronary use alone, the intracoronary and peripheral intravenous use of nicorandil can better improve myocardial microcirculation and short-term prognosis .

Nicorandil use prior and post PCI could decrease the occurrence rate of ventricular arrhythmia in STEMI patients undergoing emergent PCI, and this effect might be related with reduced QTd and QTcd post medication .

Whether oral nicorandil, which is more widely available and more affordable, would have clinical benefits in terms of measures of reperfusion, and LV recovery post-STEMI, when administered in the early phase of STEMI is still questionable, and warrants further research.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Early Administration of Oral Nicorandil in ST Elevation Myocardial Infarction Patients Undergoing Primary Percutaneous Coronary Intervention: A Randomized Controlled Trial
Anticipated Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 29, 2023

Arms and Interventions

Arm Intervention/Treatment
Group A

will receive standard treatment + 20 mg nicorandil prior to PPCI, and then maintained on 20 mg b.i.d for 3 months .

Drug: Nicorandil 20 MG
Nicorandil is a nicotinamide ester that dilates peripheral and coronary resistance vessels via action on ATP-sensitive potassium channels and possesses a nitrate moiety that promotes systemic venous and coronary vasodilation. As a result of these dual actions, nicorandil reduces preload and afterload and results in an increase in coronary blood flow. In addition to these effects, nicorandil may have cardioprotective actions mediated through the activation of potassium channel
Other Names:
  • PCI
  • Group B

    will be given standard treatment, without nicorandil loading or maintainance.

    Outcome Measures

    Primary Outcome Measures

    1. Angiographic evidence of epicardial successful reperfusion [1 day around PCI]

      Angiographic evidence of epicardil successful reperfusion including; TIMI flow grade, and TIMI frame count.

    2. Angiographic evidence of tissue-level successful reperfusion [1 day around PCI]

      Angiographic evidence of tissue-level successful reperfusion (Myocardial blush grade).

    Secondary Outcome Measures

    1. Electrocardiographic measures of repolarization dispersion [after 90 minutes of PPCI]

      Electrocardiographic measures of repolarization dispersion including; QTc, QTD, T-peak to T-end interval (Tp-Te), and its dispersion, and Tp-Te/QT ratio, as well as ST segment resolution at 90 minutes from reperfusion.

    2. Echocardiographic measures of LV recovery [before discharge and at 3 months after index event.]

      Echocardiographic measures of LV recovery including; 2-D left ventricular ejection fraction, left ventricle volumes, Mitral regurge severity, and wall motion score index.

    3. Speckle tracking for global longitudinal strain of left ventricle [before discharge and at 3 months after index event]

      2D- Left ventricle Global longitudinal strain by speckle tracking echocardiography (only 50 patients in each group)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    16 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with STEMI eligible for PPCI.
    Exclusion Criteria:
    • Patients undergoing other reperfusion strategies, including fibrinolysis, rescue PCI or pharmacoinvasive PCI.

    • Patients presenting with Cardiogenic shock or symptomatic hypotension (BP< 90/60 mmHg)

    • Patients who have contraindications for nicorandil e.g. advanced hepatic disease.

    • Patients not consenting to the study protocol.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Ahmed Abdel Nasser Abdel Rady

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Ahmed Abdel Nasser Abdel Rady, Principal Investigator, Assiut University
    ClinicalTrials.gov Identifier:
    NCT04632121
    Other Study ID Numbers:
    • Nicorandil in STEMI Patients
    First Posted:
    Nov 17, 2020
    Last Update Posted:
    Jan 5, 2021
    Last Verified:
    Jan 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2021