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NCT03311984 Clinical Trial

Anti-Xa Levels in Critically Ill Patients Receiving Low-molecular-weight Heparin for Thromboprophylaxis in China

Critically Ill Clinical Trial

Official title:
Evaluation of Anti-Xa Levels in Critically Ill Patients Receiving Low-molecular-weight Heparin for Thromboprophylaxis in China

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03311984
Other study ID # Anti-Xa Level
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 6, 2017
Last updated October 16, 2017
Start date August 15, 2017
Est. completion date May 30, 2018

Study information
Verified date October 2017
Source Southeast University, China
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Critically ill Patients are at high risk to develop deep venous thrombosis. However, despite receiving of a standard dose of Low-molecular-weight Heparin（LMWH）, many patients still develop life-threatening embolism. The purpose of this study is to evaluate the anti-Xa levels of different dosing regimens of LMWH in critically ill patients in China.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 200
Est. completion date May 30, 2018
Est. primary completion date March 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult Critically ill patients

Exclusion Criteria:

- Contraindication to use of LMWH. Intracranial bleeding/stroke, hematoma or bleeding disorder. Use Heparin anticoagulant therapy

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• anti Xa level
monitoring the anti-Xa level according to LMWH emploing

Locations
Country Name City State
China Changde Wu Nanjing Jiangsu

Sponsors (1)
Lead Sponsor Collaborator
Southeast University, China

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Anti-Xa Levels six months
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