NCT02213978CompletedNot 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 enrollmentStarted: August 2014Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 1,114
- Locations
- 1
- Primary Endpoint
- the incidence of venous thromboembolism under the thromboprophylaxis in critical ill patients
Study 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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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)
Investigators
Xiao Tang
doctor of the department of respiratory and critical care medicine of Beijing Chao Yang Hospital
Beijing Chao Yang Hospital
Study Sites (1)
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