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
| Type | Name | Description |
|---|---|---|
| DRUG | nafamostat mesilate | Use nafamostat mesilate as an anticoagulant |
| DRUG | unfractionated heparin group | Use 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.