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

Venous Thromboembolism Clinical Trial

— VTEH  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02213978
• Other study ID #: ICU-VTE-2014
• Status: Completed
• Start date: August 2014
• Est. completion date: December 2021

Study information

• Verified date: January 2022
• Source: Beijing Chao Yang Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial 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.

Recruitment information / eligibility

• 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

Related Conditions & MeSH terms

• Hemorrhage
• Thromboembolism
• Venous Thromboembolism

Locations

Country	Name	City	State
China	Department of respiratory and critical care medicine,Beijing Chao-yang Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Beijing Chao Yang Hospital

Country where clinical trial is conducted

China, 

Outcome

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