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Clinical Trials/NCT02213978
NCT02213978
Completed
Not Applicable

A Clinical Cohort Study of Safety and Effectiveness of Venous Thromboembolism Prophylaxis in Critical Ill Patients

Beijing Chao Yang Hospital1 site in 1 country1,114 target enrollmentAugust 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Venous Thromboembolism
Sponsor
Beijing Chao Yang Hospital
Enrollment
1114
Locations
1
Primary Endpoint
the incidence of venous thromboembolism under the thromboprophylaxis in critical ill patients
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to analyze the effect of the prophylaxis of venous thromboembolism in the critical ill patients, and at the same time, to find out the risk of venous thromboembolism and hemorrhage events occurred under the prophylaxis.

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
December 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Beijing Chao Yang Hospital
Responsible Party
Principal Investigator
Principal Investigator

Xiao Tang

doctor of the department of respiratory and critical care medicine of Beijing Chao Yang Hospital

Beijing Chao Yang Hospital

Eligibility Criteria

Inclusion Criteria

  • all the patients in ICUs estimated time in ICU mare than 48h

Exclusion Criteria

  • estimated time in ICU less than 48h refused to attend

Outcomes

Primary Outcomes

the incidence of venous thromboembolism under the thromboprophylaxis in critical ill patients

Time Frame: 2 weeks

at the same time, to analyze the risk factor of the occurrence of venous thromboembolism despite of thromboprophylaxis

Secondary Outcomes

  • the incidence of bleeding events under thromboprophylaxis in critical ill patients(2 weeks)

Study Sites (1)

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