Nafamostat Mesilate in the Treatment of Severe Infection-associated Coagulopathy
NCT06078839 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 778
Last updated 2023-10-12
Summary
The objective of this study was to evaluate the therapeutic effect of nafamostat mesilate on patients with severe infection-related coagulation。
Conditions
- Sepsis
- Sepsis-induced Coagulopathy
- Nafamostat Mesilate
Interventions
- DRUG
-
Nafamostat mesilate
Nafamostat 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)
- DRUG
-
5% glucose
Add 50ml of 5% glucose into a 50ml syringe
Sponsors & Collaborators
-
Tianjin Third Central Hospital
collaborator OTHER -
Tianjin Medical University General Hospital
collaborator OTHER -
Shanxi Provincial People's Hospital
collaborator OTHER_GOV -
Shanxi Bethune Hospital
collaborator OTHER -
Hohhot First Hospital
collaborator UNKNOWN -
The First Bethune Hospital Jilin University
collaborator UNKNOWN -
Northern Jiangsu People's Hospital
collaborator OTHER -
The Affiliated Hospital of Nantong University
collaborator UNKNOWN -
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
collaborator OTHER -
The First Affiliated Hospital of Suzhou Medical
collaborator UNKNOWN -
Anhui Provincial Hospita
collaborator UNKNOWN -
Zhejiang Hospital
collaborator OTHER -
Zhejiang Provincial People's Hospital
collaborator OTHER -
The First Affiliated Hospital of Ningbo
collaborator UNKNOWN -
The First Affiliated Hospital of Wenzhou
collaborator UNKNOWN -
The Jiangxi Provincial People's Hospital
collaborator UNKNOWN -
First Affiliated Hospital of Gannan Medical University
collaborator OTHER -
The Second Affiliated Hospital Xi'an Jiaotong
collaborator UNKNOWN -
LanZhou University
collaborator OTHER -
The First Affiliated Hospital of Xinjiang
collaborator UNKNOWN -
First Affiliated Hospital of Xinjiang Medical University
collaborator OTHER -
Tongji Medical College of Huazhong University
collaborator UNKNOWN -
The Second Hospital University of South China
collaborator OTHER -
The Fourth Affiliated Hospital of China Medical
collaborator UNKNOWN -
The First Affiliated Hospital of Liaoning
collaborator UNKNOWN -
Genertec Liaoyou Gem Flower Hospital
collaborator UNKNOWN -
The Tenth People's Hospital of Shenyang
collaborator UNKNOWN -
The Sixth People's Hospital of Shenyang
collaborator OTHER -
Dalian NO.3 People's Hospital
collaborator UNKNOWN -
Benxi Cental Hospital
collaborator OTHER -
Liaoyang City Central Hospital
collaborator UNKNOWN -
Huludao central hospital
collaborator UNKNOWN -
Xu Li
lead OTHER
Principal Investigators
-
Xu Li, Phd · First Hospital of China Medical University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-10-01
- Primary Completion
- 2026-10-01
- Completion
- 2026-10-01
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