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Clinical Trial Summary

This randomized, multi-center, double-blinded, placebo-controlled study is designed to evaluate the efficacy and safety of milrinone compared with placebo in participants after corrective surgery for congenital heart disease. Participants will be randomized in a 1:1 ratio within 90 minutes after arriving in the intensive care unit (ICU), to receive either intravenous milrinone or placebo for 36 hours. Participants will be stratified according Vasoactive Inotrope Score after arriving in the ICU.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03823781
Study type Interventional
Source Shanghai Children's Medical Center
Contact Jihong Huang, MD, PhD
Phone +8618930830766
Email huangjihong@scmc.com.cn
Status Recruiting
Phase Phase 3
Start date February 2019
Completion date July 2021

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