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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02213978
Acronym
VTEH
Enrollment
1114
Registered
2014-08-12
Start date
2014-08-31
Completion date
2021-12-31
Last updated
2022-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemorrhage, Venous Thromboembolism

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.

Interventions

None listed

Sponsors

Beijing Chao Yang Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
the incidence of venous thromboembolism under the thromboprophylaxis in critical ill patients2 weeksat the same time, to analyze the risk factor of the occurrence of venous thromboembolism despite of thromboprophylaxis

Secondary

MeasureTime frameDescription
the incidence of bleeding events under thromboprophylaxis in critical ill patients2 weeksat the same time, to analyze the risk factors of bleeding in critical ill patients who receive thromboprophylaxis

Other

MeasureTime frameDescription
the incidence of venous thromboembolism under the mechanical thromboprophylaxis in the critical ill patients who with the contraindications to anticoagulation2 weeksAt the same time,to analyze the aspects below: 1. Evaluation the tolerance to mechanical thromboprophylaxis of these patients 2. Comparison of the effectiveness between intermittent pneumatic compression and graduated compression stockings in mechanical thromboprophylaxis

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026