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Completed

NCT Number: NCT04573751

The EPIVER Randomized Controlled Trial

The trial aims to estimate the efficacy and safety of the intracoronary administration of adrenalin, verapamil, as well as their combination compared to standard treatment in patients with STEMI and refractory coronary no-reflow despite conventional treatment during percutaneous coronary intervention (PPCI)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cardiology Research Institute, Tomsk NRMC

Tomsk, Tomsk Oblast, Russia

About this study

Primary percutaneous coronary intervention (PPCI) is the preferred reperfusion strategy for treating acute ST-segment elevation myocardial infarction (STEMI). The main goals are to restore epicardial infarct-related artery patency and to achieve microvascular reperfusion as early as possible. No-reflow is the term used to describe inadequate myocardial perfusion of a given coronary segment without angiographic evidence of persistent mechanical obstruction of epicardial vessels and it refers to the high resistance of microvascular blood flow encountered during opening of the infarct-related coronary artery. Despite optimal evidence-based PPCI, myocardial no-reflow can still occur, negating many of the benefits of restoring culprit vessel patency, and is associated with a worse in-hospital and long-term prognosis.

According to clinical guidelines, nitrates, adenosine, platelet IIb / IIIa receptor inhibitors and thrombus extraction can be used to prevent and treat this complication.These methods have demonstrated the ability to improve coronary blood flow in experiment and small clinical trials, however, limiting the zone of myocardial necrosis and improving disease outcomes have not been achieved.

The search for new methods of influencing the pathogenetic links of this complication is urgent. One of the main potentially reversible factors in the pathogenesis of the no-reflow phenomenon, along with microvascular obstruction, is microvascular arteriolar spasm. Thus, this problem of emergency cardiology remains relevant and requires further research, new methods of prevention and treatment.

Aside from exerting beta-1 agonist properties at higher doses and increasing the inotropic and chronotropic stimulation of the myocardium, epinephrine may, at lower doses, exert potent beta receptor agonist properties that mediate coronary vasodilatation. Another drug with a pronounced coronary vasodilation effect is verapamil.

Based on the pharmacodynamic effects of epinephrine and verapamil, it is expected to increase the vasodilating effect when they are used together, due to the additive type of synergistic interaction, which will improve coronary microcirculation after PCI in patients with acute myocardial infarction and refractory no-reflow phenomenon.

Currently, in clinical practice, there is a possibility of very sensitive diagnosis of microvascular obstruction (MVO) using magnetic resonance imaging (MRI), as well as the area of the coronary reserve according to dynamic perfusion scintigraphy of the myocardium. It is advisable to evaluate the effectiveness of treatment of the no-reflow phenomenon using these methods.

The trial aims to estimate the efficacy and safety of the administration of intracoronary epinephrine, verapamil, as well as their combination versus to standard treatment in patients with STEMI and refractory coronary no-reflow despite conventional treatments during PPCI.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients with ST-elevation myocardial infarction
  • Infarct-related artery TIMI flow grade 0-2 during the interventional procedure after the initial opening of the vessel.
  • Written the informed consent to participate in research

Exclusion criteria

  • Unable to undergo or contra-indications for MRI or SPECT

Treatment and study plan

Standard therapy

Drug

Standard therapy as follows: adenosine, nitroglycerine, thrombus aspiration/extraction, and platelet IIb/IIIa receptor inhibitors.

Other names: Control

Epinephrine

Drug

Standard therapy plus epinephrine as follows: epinephrine, adenosine, nitroglycerine, thrombus aspiration/extraction, and platelet IIb/IIIa receptor inhibitors.

Other names: Epi

Verapamil

Drug

Standard therapy plus verapamil as follows: verapamil, adenosine, nitroglycerine, thrombus aspiration/extraction, and platelet IIb/IIIa receptor inhibitors.

Other names: Ver

Epinephrine + verapamil

Drug

Standard therapy plus epinephrine + verapamil as follows: epinephrine, verapamil, adenosine, nitroglycerine, thrombus aspiration/extraction, and platelet IIb/IIIa receptor inhibitors.

Other names: Epi+Ver

Primary outcomes

  1. Mortality

    Time frame: month 1

    Mortality rate (percent)

  2. New onset or worsening acute heart failure

    Time frame: month 1

    The rate (percent) of patients experiencing new onset or worsening acute heart failure. Congestion characterized by dyspnea, edema, rales, jugular venous distention and need to increase diuretic doses is a hallmark of acute heart failure prompting hospitalization

Secondary outcomes

  1. Thrombolysis in myocardial infarction (TIMI) 3

    Time frame: hour 1

    The rate of patients (percent) who achieved TIMI 3 coronary blood flow after percutaneous coronary intervention

  2. Change in systolic/diastolic blood pressure

    Time frame: minute 3

    Change in systolic/diastolic blood pressure values (mmHg) before and after intracoronary verapamil/epinephrine

  3. ST segment resolution

    Time frame: hour 72

    Degree of ST segment resolution on ECG (mm)

  4. Troponin I release

    Time frame: hour 72

    Concentration of troponin I (ng/mL)

  5. LV EF

    Time frame: day 10

    Left ventricular ejection fraction (LV EF) (percent)

  6. Myocardial injury

    Time frame: day 2

    Total volume (mL) of microvascular obstruction, myocardial necrosis, edema, and hemorrhagic impregnation according to MRI data

  7. SPECT-based coronary reserve

    Time frame: day 7

    Coronary reserve will be measured by cardiac single photon emission computed tomography (SPECT) with technetium-99m-labeled methoxy-isobutyl isonitrile (99mТсMIBI) at rest and during pharmacological stress-test (counts)

  8. Change in heart rate values

    Time frame: minute 3

    Change in heart rate values (beat per minute) before and after intracoronary verapamil/epinephrine

  9. LV EDV

    Time frame: 10 days

    Left ventricular end-diastolic volume (LV EDV) (mL)

  10. LV ESV

    Time frame: day 10

    Left ventricular end-systolic volume (LV ESV) (mL)

  11. LV WMSI

    Time frame: day 10

    Left ventricular wall motion score index (LV WMSI) (conventional units)

  12. Arrhythmias

    Time frame: minute 5

    Frequency of arrhythmias (atrial fibrillation, atrial flutterу, supraventricular tachycardia, premature ventricular contractions, ventricular tachycardia, conduction disorders and other heart rhythm disorders) after intracoronary administration verapamil and/or epinephrine

Sponsors and collaborators

Lead sponsor

Tomsk National Research Medical Center of the Russian Academy of Sciences

Other

Registry information

Official study title

Intracoronary Administration of Epinephrine and Verapamil in the Refractory No-reflow Phenomenon in Patients With Acute Myocardial Infarction: The EPIVER Randomized Controlled Trial

Acronym: EPIVER

Important dates

Study start
2020
Primary completion
2023
Study completion
2024
First posted
Oct 5, 2020
Registry last updated
Jun 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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