Prophylactic Use of Milrinone After Congenital Heart Surgery in Infants

Status Recruiting

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

Clinical Trial Details

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

View Details

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