Venous Thromboembolism Clinical Trial
— VTEHOfficial title:
A Clinical Cohort Study of Safety and Effectiveness of Venous Thromboembolism Prophylaxis in Critical Ill Patients
NCT number | NCT02213978 |
Other study ID # | ICU-VTE-2014 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | August 2014 |
Est. completion date | December 2021 |
Verified date | January 2022 |
Source | Beijing Chao Yang Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
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.
Status | Completed |
Enrollment | 1114 |
Est. completion date | December 2021 |
Est. primary completion date | December 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
China | Department of respiratory and critical care medicine,Beijing Chao-yang Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Beijing Chao Yang Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | the incidence of venous thromboembolism under the mechanical thromboprophylaxis in the critical ill patients who with the contraindications to anticoagulation | At the same time,to analyze the aspects below:
Evaluation the tolerance to mechanical thromboprophylaxis of these patients Comparison of the effectiveness between intermittent pneumatic compression and graduated compression stockings in mechanical thromboprophylaxis |
2 weeks | |
Primary | the incidence of venous thromboembolism under the thromboprophylaxis in critical ill patients | at the same time, to analyze the risk factor of the occurrence of venous thromboembolism despite of thromboprophylaxis | 2 weeks | |
Secondary | the incidence of bleeding events under thromboprophylaxis in critical ill patients | at the same time, to analyze the risk factors of bleeding in critical ill patients who receive thromboprophylaxis | 2 weeks |
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