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Completed

NCT Number: NCT01318460

Prophylactic Administration of Levosimendan in Patients Undergoing Coronary Surgery

The present pilot study aims to investigate the effectiveness of the preoperative infusion of levosimendan in patients with impaired left ventricular function undergoing coronary artery bypass grafting.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Cardiothoracic Surgery, AHEPA University Hospital

Thessaloniki, 546 36, Greece

About this study

Myocardial revascularization in patients with impaired left ventricular function remains a serious problem in cardiac surgery. Despite the recent developments with the use of new surgical techniques (mini-extracorporeal circulation, off pump surgery) the perioperative morbidity and mortality are relatively high. Therapeutic solutions with the use of inotropic drugs, as adrenergic agonists and phosphodiesterase inhibitors, have offered important improvement to the hemodynamic status of these patients, but they have not considerably decreased mortality. These drugs owe their positive inotropic action to the increase of intracellular calcium and thereafter they improve the myocardial function.

Levosimendan (SIMDAX) is a new calcium sensitizer which increases the myocardial contractility without particular promotion of the intracellular calcium accumulation. Contemporary experimental and clinical data demonstrated the effectiveness of this drug in the reduction of surgical mortality to the patients with low left ventricular ejection fraction (LVEF) who undergo coronary artery bypass grafting (CABG).

This is an original prospective randomized controlled study focused on the preoperative use of this drug in patients with impaired left ventricular function which is associated with a high operative risk (i.e. EuroSCORE). Perioperative myocardial stunning is particularly evident in this cohort of patients. Prophylactic administration of levosimendan the day before the operation could be translated in improved myocardial performance intraoperatively and during the early postoperative period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • coronary artery disease which warrants myocardial revascularization with coronary artery bypass grafting according to current guidelines
  • age < 79 years old
  • left ventricular ejection fraction <= 40%
  • informed patient's consent

Exclusion criteria

  • age < 18 years old
  • emergency surgery
  • medical history of acute myocardial infarction with ST elevation (STEMI) less than 14 days old
  • any severe comorbidity which increases the perioperative risk (i.e. neoplasia, rheumatoid arthritis, chronic obstructive pulmonary disease)
  • need for valvular replacement surgery
  • redo surgery
  • serum creatinine > 2 mg/dl
  • history of malignant cardiac arrhythmias

Treatment and study plan

Levosimendan infusion

Drug

Prophylactic 24h infusion of levosimendan at a dose of 0.1 mg/kg/min

placebo infusion

Drug

Twenty-four hour administration of placebo

Primary outcomes

  1. Left ventricular function

    Time frame: Seventh postoperative day

    Left ventricular function as assessed by transthoracic or transesophageal echocardiography on the seventh postoperative day

Secondary outcomes

  1. Perioperative mortality

    Time frame: 30 days postoperatively

  2. Need for intraaortic balloon pump

    Time frame: 1st-7th postoperative day

  3. Inotropic support

    Time frame: 1st-7th postoperative day

    Need for high inotropic support

  4. Total ICU stay

    Time frame: 1st-7th postoperative day

  5. Total length of hospital stay

    Time frame: 1st-7th postoperative day

  6. Time on mechanical ventilation

    Time frame: 1st-7th postoperative day

  7. Major adverse cardiovascular events

    Time frame: 1st-7th postoperative day

    Perioperative myocardial infarction, stroke, need for revascularization)

  8. Morbidity

    Time frame: 1st-7th postoperative day

Sponsors and collaborators

Lead sponsor

AHEPA University Hospital

Other

Collaborators

  • Orion Corporation, Orion Pharma

Registry information

Official study title

Prophylactic Administration of Levosimendan in Patients With Impaired Left Ventricular Function Undergoing Coronary Surgery

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Mar 18, 2011
Registry last updated
May 7, 2019

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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