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Completed

NCT Number: NCT03557255

Levosimendan for Cardiac Patients Undergoing Major Abdominal Cancer Surgeries

The objective of this pilot study is to evaluate the efficacy and safety of preoperative administration of levosimendan in patients with chronic heart failure scheduled for major abdominal cancer surgery assuming the reduction of both perioperative morbidity and mortality.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Anesthesia and Pain medicine.National Cancer Institute

Cairo, 11796, Egypt

About this study

Cardiac complications are one of the most common causes of perioperative morbidity and mortality in patients undergoing non-cardiac surgery. Heart failure (HF) is an established risk factor for postoperative cardiac complications and mortality. The risk for postoperative mortality following major non-cardiac surgery is twice as that of patients with coronary artery disease (CAD) without HF. HF occurs in 1% to 6% of patients after major surgery, the risk being higher, between 6% and 25%, in patients with pre-existing cardiac conditions such as CAD, prior HF or valvular heart disease.

Cardiovascular disease and cancer are among the leading causes of mortality worldwide. The number of patients presenting with both diseases concomitantly is likely to increase. Cardiac patients undergoing major abdominal cancer surgeries with substantial fluid shift, blood loss and severe hemodynamic instability are at higher risk for perioperative HF.Therefore, preoperative optimization of such patients is of paramount importance. Unfortunately, guidelines for the perioperative management and preparation of such patients have not been proposed. Besides, the prophylactic use of inotropic agents for preoperative optimization of patients at high risk for HF remains controversial owing to their potential to jeopardize the myocardial oxygen supply-demand balance or to induce dysrhythmias with an assumed higher mortality.

Levosimendan is a calcium sensitizer with a positive inotropic action that has been shown to safely improve cardiac performance and hemodynamics in HF patients without increasing the myocardial oxygen demand or causing dysrrhythmias. The perioperative use of levosimendan for optimization of patients with HF has been reported in few studies with promising results, mainly for cardiac patients undergoing cardiac surgeries. However, the role of levosimendan has not been thoroughly evaluated in patients with chronic heart failure (CHF) undergoing major cancer surgery.

The purpose of this prospective study is to evaluate the safety and efficacy of preoperative administration of levosimendan in patients with CHF scheduled for major abdominal cancer surgery.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients suffering from CHF with left ventricular ejection fraction < 35%, scheduled for major abdominal cancer surgery were eligible.
  • Aged 18 to 75 years.

Exclusion criteria

were :

  • restrictive or obstructive cardiomyopathy.
  • severe cardiac valvular disease.
  • history of atrial fibrillation, ventricular tachycardia or fibrillation.
  • resting systolic arterial pressure <80 mmHg.
  • second or third degree atrioventricular block.
  • Child-Pugh class C liver cirrhosis.
  • severe renal failure (defined as creatinine clearance < 30 ml/min).
  • Immediate postoperative complications such as surgical re-exploration for bleeding or suspected leak.

Treatment and study plan

Levosimendan

Drug

Preoperative 24 hours infusion of levosimendan for chronic heart failure patients prior to major abdominal cancer surgeries.

Other names: drug group

Saline

Drug

Preoperative 24 hours infusion of normal saline for chronic heart failure patients prior to major abdominal cancer surgeries.

Other names: control group

Primary outcomes

  1. Changes in mechanical ventilation

    Time frame: Baseline and after two weeks

    The total duration of postoperative ventilation in days

Secondary outcomes

  1. Changes in Ejection fraction

    Time frame: Baseline and after one week postoperative

    The improvement in the ejection fraction in percentage.

  2. Changes in cardiac index

    Time frame: Baseline and after one week postoperative

    The improvement in Cardiac index (Liters/minute/square meter)

  3. Changes in Stroke volume index

    Time frame: Baseline and after one week postoperative

    The improvement in stroke volume index(milliliters/square meter)

  4. Patient total hospital length of stay

    Time frame: Baseline and after two weeks postoperative

    Total hospital length of stay in days.

Sponsors and collaborators

Lead sponsor

National Cancer Institute, Egypt

Other

Registry information

Official study title

The Role of Preoperative Use of Levosimendan in Ischemic Cardiac Patients Undergoing Major Abdominal Cancer Surgeries: A Prospective Randomized Study

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jun 14, 2018
Registry last updated
Jun 14, 2018

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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