Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06276010

Use of Nafamostat Mesilate for Anticoagulation in Patients With ECMO

Use of Nafamostat Mesilate for Anticoagulation in Patients With Extracorporeal Membrane Oxygenation After Cardiac Surgery: Efficacy and Safety

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Xiaotong Hou · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effectiveness and safety of nafamostat mesilate compared with unfractionated heparin for anticoagulation in patients with ECMO after cardiac surgery.

Detailed description

Selecting patients who require systemic anticoagulation as the study subjects from patients undergoing extracorporeal membrane oxygenation assistance after cardiac surgery. Randomly divided into the nafamostat mesilate group and unfractionated heparin group. To evaluate the efficacy and safety of nafamostat mesilate by comparing the incidence of bleeding and thrombosis within the target anticoagulant level range between two groups of patients during ECMO

Conditions

Interventions

TypeNameDescription
DRUGnafamostat mesilateUse nafamostat mesilate as an anticoagulant
DRUGunfractionated heparin groupUse unfractionated heparin as an anticoagulant

Timeline

Start date
2024-07-01
Primary completion
2026-11-01
Completion
2026-12-31
First posted
2024-02-23
Last updated
2025-09-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06276010. Inclusion in this directory is not an endorsement.

Use of Nafamostat Mesilate for Anticoagulation in Patients With ECMO (NCT06276010) · Clinical Trials Directory