Levosimendan
DrugThe drug infusion will be started after initiation of cardiopulmonary bypass and will continue for 24 hours.
Other names: Simdax
NCT Number: NCT02232399
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).
Looking for future studies?
Notify Me1 month–12 month
All sexes
Interventional
Phase 2
Children´s Hospital, Helsinki University Central Hospital, Helsinki, Finland
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The drug infusion will be started after initiation of cardiopulmonary bypass and will continue for 24 hours.
Other names: Simdax
The drug infusion will be started after initiation of cardiopulmonary bypass and will continue for 24 hours.
Other names: Corotrop
Time frame: One day after cardiac surgery
The primary outcome variable was the absolute value of serum creatinine data on postoperative day 1.
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)
Time frame: 30 days
Mortality at 30th day
Göteborg University
Other
The Prophylactic Effect of Levosimendan in Reducting Acute Kidney Injury Postoperatively in Pediatric Patients Undergoing Corrective Heart Surgery
Acronym: MiLe-1
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.
NCT03822442
Cardiac Imaging Techniques, Cardiomegaly
Washington D.C., District of Columbia, United States
View Trial DetailsNCT01845402
Cardiovascular Abnormalities, Cardiovascular Diseases
Paris, France
View Trial DetailsNCT02320669
Cardiovascular Abnormalities, Cardiovascular Diseases
Los Angeles, California, United States
View Trial DetailsNCT00740870
Cardiovascular Abnormalities, Cardiovascular Diseases
Miami, Florida, United States
View Trial Details