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Efficacy and Safety of Nafamostat Mesylate for VV-ECMO Anticoagulation

Critical Illness Clinical Trial

Official title:
Efficacy and Safety of Nafamostat Mesylate for VV-ECMO Anticoagulation: a Randomized, Single-blind, Multicenter Exploratory, Heparin-controlled Trial

Clinical Trial Summary

The purpose of this study was to compare the efficacy and safety of nafamostat mesylate and unfractionated heparin during ECMO anticoagulation in critically ill patients.

Clinical Trial Description

During ECMO treatment, nafamostat mesylate and unfractionated heparin were randomly administered for continuous anticoagulation, respectively, and the incidence of bleeding and thrombotic complications during anticoagulation was compared between the two groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05555641
Study type Interventional
Source Wuhan Union Hospital, China
Contact You Shang, Prof.
Phone 008602785351607
Email you_shanghust@163.com
Status Recruiting
Phase Phase 2
Start date December 20, 2022
Completion date October 1, 2024
View Details
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