Clinical Trials Directory

Trials / Completed

CompletedNCT05221879

Anti-factor Xa Based Venous Thromboembolism Prophylaxis

Anti-factor Xa Based Venous Thromboembolism Prophylaxis: Dose Adjustment in ICU Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
75 (actual)
Sponsor
Meir Medical Center · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Introduction: Venous thromboembolism (VTE) in the intensive care unit (ICU) is associated with significant morbidity and mortality therefore prevention is imperative to reduce its burden. VTE prophylaxis in ICU patients is primarily pharmacological using low molecular weight heparin. This study aims to determine the proportion of ICU patients receiving VTE prophylaxis that achieves appropriate anti-factor Xa activity (aFXa) prophylactic levels and to characterize this patient population Methods: Seventy-five patients admitted to the General ICU were included. Peak and trough aFXa levels were measured at 4 and 23 hours respectively after receiving the second consecutive daily enoxaparin 40 mg sc injection. Patients in whom peak aFXa levels were found to be sub-prophylactic, peak and trough levels were repeated as above

Conditions

Interventions

TypeNameDescription
OTHERDose adjustment of Enoxaparin in patients with sub-therapuetic (prophylactic) levels of factor 10aWe screened ICU patients who recieved DVT prophylaxis with fixed dose of Enoxaparin (40 mg SC daily) for peak blood levels of factor 10A. For patients who did not achieve therapuetic 10a levels (0.2-0.4) we increased the Enoxaparin dose to 60 mg SC daily.

Timeline

Start date
2019-06-23
Primary completion
2021-02-15
Completion
2021-02-15
First posted
2022-02-03
Last updated
2022-02-03

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT05221879. Inclusion in this directory is not an endorsement.