Skip to main content
OpenTrials
Completed

NCT Number: NCT02232399

Is Levosimendan Superior to Milrinone Regarding Acute Kidney Injury After Cardiac Surgery for Congenital Heart Disease?

The aim of the study is to assess the ability of Levosimendan to reduce the postoperative acute kidney injury in pediatric patients undergoing surgery for congenital heart disease (CHDs).

Completed

Looking for future studies?

Notify Me

Key information

Age range

1 month–12 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Children´s Hospital, Helsinki University Central Hospital, Helsinki, Finland

Loading trial locations.

About this study

Young children, between the age of 1 to 12 months, with congenital heart disease in need of elective heart surgery will be included in this study.

The trial will contain two study groups, 35 patients in each. One group will receive Levosimendan and the second group will receive Milrinone as a heart muscle-strengthening agent during and after the operation. Milrinone is currently used as the drug of choice in many pediatric cardiac surgery centers. It remains to see if Levosimendan can exert a kidney protecting function in addition to its heart muscle-strengthening properties.

The primary objective of this study is to investigate the preventive effect of Levosimendan on postoperative acute kidney injury in pediatric patients undergoing surgery for their CHDs. Creatinine levels postoperatively will be the primary endpoint. Creatinine, the common marker of kidney injury, will be measured daily.

The treatment with Levosimendan or Milrinone will be started during the operation (after initiation of cardiopulmonary bypass) and will last 24 hours. Blood samples will be obtained at six occasions perioperatively. Patients will be followed 4 days after termination of treatment (totally 5 days).

The duration of study will be 30 days (24 hours treatment + 4 days follow up + 30-days-mortality registration).

Creatinine is the primary outcome in this study. Inflammatory biomarkers and other relevant biomarkers will comprise the secondary outcome variables.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Provision of informed consent prior to any study specific procedures
  • Female and male children between 1 and 12 months of age
  • Non-restrictive VSD (corrective surgery)
  • Complete AVSD (biventricular repair)
  • Tetralogy of Fallot

Exclusion criteria

  • Unbalanced AtrioVentricular Septal Defect or AVSD with cyanosis
  • Age less than one month and more than one year
  • Acute operation that is unscheduled operation during the first 24 hours after presentation to the department for thoracic surgery
  • Mild, moderate, or severe kidney dysfunction and known anatomical anomalies of kidneys
  • Liver impairment or disease
  • Ongoing infection
  • Use of nephrotoxic drugs (like ibuprofen, angiotensin-converting-enzyme inhibitors, gentamicin, vancomycin) preoperative or postoperative until first post operative day. Contrast agents whithin 24 hours before operation.
  • Use of inhibitors of membrane transport proteins (cimetidine, cetirizine, trimethoprim, probenecid, rifampin and gemfibrosil).
  • Allergy to Levosimendan or substance included in the preparation or previous use of Levosimendan.
  • Severe arrhythmias needing pace-maker treatment prior to the operation
  • Severe cardiac dysfunction needing for treatment with extracorporeal membrane oxygenation (ECMO) prior to the operation.
  • Preoperative need for mechanical ventilation and/or inotropic agents.
  • Re-operation (open heart surgery). Earlier surgical closure of the arterial duct does not count as an exclusion criteria.
  • Prematurity: Gestational age < 30 weeks, irrespective of postpartum age. Gestational age 30-34 weeks if patient is included at postpartum age under 3 months.

Treatment and study plan

Levosimendan

Drug

The drug infusion will be started after initiation of cardiopulmonary bypass and will continue for 24 hours.

Other names: Simdax

Milrinone

Drug

The drug infusion will be started after initiation of cardiopulmonary bypass and will continue for 24 hours.

Other names: Corotrop

Primary outcomes

  1. S-creatinine

    Time frame: One day after cardiac surgery

    The primary outcome variable was the absolute value of serum creatinine data on postoperative day 1.

Secondary outcomes

  1. Acute Kidney Injury (AKI)

    Time frame: Two days (second postoperative day)

    Secondary outcomes included the occurrence rate of AKI, defined as a 50% rise in serum creatinine, or more, within 48 hours after surgery. All stages of AKI (stage 1 and stage 2 and stage 3)

  2. 30 Days Mortality

    Time frame: 30 days

    Mortality at 30th day

Sponsors and collaborators

Lead sponsor

Göteborg University

Other

Collaborators

  • Helsinki University Central Hospital

Registry information

Official study title

The Prophylactic Effect of Levosimendan in Reducting Acute Kidney Injury Postoperatively in Pediatric Patients Undergoing Corrective Heart Surgery

Acronym: MiLe-1

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Sep 5, 2014
Registry last updated
Mar 26, 2024

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.

Published trials that share one or more normalized conditions with this study.