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Clinical Trials/NCT01504087
NCT01504087
Unknown
Not Applicable

Using Inflammatory Markers to Predict the Development and Outcome of Venous Thromboembolism in an Intensive Care Unit

National Taiwan University Hospital1 site in 1 country200 target enrollmentMay 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Venous Thromboembolism
Sponsor
National Taiwan University Hospital
Enrollment
200
Locations
1
Primary Endpoint
deep venous thrombosis by ultrasound
Last Updated
14 years ago

Overview

Brief Summary

Venous thromboembolism (VTE) is one of the major public health problems in Western country. More than 100,000 Americans die each year from VTE. VTE is also a common complication of critical illness,1-2 and probably related to poor outcome in this patient group. Although there are guidelines about VTE prophylaxis in acutely ill medical patients and patients in medical ICU3, they are overlooked in our daily practice frequently in our country. There are many reasons for our common practice, including inadequate knowledge for the ICU physicians, more patients with bleeding tendency in ICU and low prevalence of VTE in our (eastern) country. However, the true prevalence of VTE in ICU and if thromboprophylaxis still needed in certain high risk patients are not unknown. Besides, if there is a difference in the VTE rate between western and eastern patients, what is the underlying mechanism? The major objective of this application is to answer the first part of the problem, i.e. to delineate the scope of this problem.

The specific aims of this application are as follows:

  • prevalence of venous thromboembolism in ICU in Taiwan
  • specific risk in subgroups of ICU patients
  • prevalence and risk factors for silent pulmonary embolism
Registry
clinicaltrials.gov
Start Date
May 2011
End Date
TBD
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All patients admitted to medical ICU with age over 18 y/o are eligible

Exclusion Criteria

  • Patients who do not sign the informed consent will be excluded from this study

Outcomes

Primary Outcomes

deep venous thrombosis by ultrasound

Time Frame: day 14 after ICU admission

Secondary Outcomes

  • any clinical thromboembolic event(day 14)

Study Sites (1)

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