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

No results posted yet for this study

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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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06078839 on ClinicalTrials.gov