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Not Yet RecruitingNCT06078839

Nafamostat Mesilate in the Treatment of Severe Infection-associated Coagulopathy

Nafamostat Mesilate in the Treatment of Severe Infection-associated Coagulopathy: a Multicenter Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
778 (estimated)
Sponsor
Xu Li · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

The objective of this study was to evaluate the therapeutic effect of nafamostat mesilate on patients with severe infection-related coagulation。

Conditions

Interventions

TypeNameDescription
DRUGNafamostat mesilateNafamostat mesilate treatment group was dissolved with 5% glucose at the dosage of 2.0mg/kg/ day to a total of 50ml(Maximum concentration 10mg/ml)
DRUG5% glucoseAdd 50ml of 5% glucose into a 50ml syringe

Timeline

Start date
2023-10-01
Primary completion
2026-10-01
Completion
2026-10-01
First posted
2023-10-12
Last updated
2023-10-12

Source: ClinicalTrials.gov record NCT06078839. Inclusion in this directory is not an endorsement.