Trials / Not Yet Recruiting
Not Yet RecruitingNCT06994312
The Impact of Nafamostat Mesylate on the Prognosis of Patients With Sepsis-Induced Coagulopathy Undergoing Hemofiltration
The Impact of Nafamostat Mesylate on the Prognosis of Patients With Sepsis-Induced Coagulopathy Undergoing Hemofiltration:A Single-Center, Prospective, Randomized Controlled Trial
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 282 (estimated)
- Sponsor
- The First Hospital of Jilin University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
In sepsis, the body is prone to coagulation system disorders, which may progress to sepsis-induced coagulopathy (SIC). When SIC is persistent and cannot be corrected, it often sequentially develops into disseminated intravascular coagulation (DIC) with multiple organ failure. Nafamostat mesylate can be used as an anticoagulant during blood purification in critically ill patients and is also used to treat SIC.Safe and effective anticoagulation is a prerequisite for the success of blood purification therapy. For patients with active bleeding or at risk of bleeding, how to achieve extracorporeal anticoagulation without affecting the body's coagulation function is a major clinical challenge. Nafamostat mesylate can reduce the risk of bleeding during blood purification, but its impact on the survival outcomes of patients with SIC undergoing blood purification therapy remains unclear.The aim of this study is to evaluate the impact of nafamostat mesylate treatment on the prognosis of patients with sepsis-induced coagulopathy undergoing hemofiltration.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nafamostat Mesylate | Anticoagulation with Nafamostat Mesylate for SIC Patients Undergoing Hemofiltration |
| DRUG | sodium citrate | Anticoagulation with Sodium Citrate for SIC Patients Undergoing Hemofiltration |
Timeline
- Start date
- 2025-07-01
- Primary completion
- 2028-05-01
- Completion
- 2028-12-01
- First posted
- 2025-05-29
- Last updated
- 2025-05-29
Source: ClinicalTrials.gov record NCT06994312. Inclusion in this directory is not an endorsement.