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
| Type | Name | Description |
|---|---|---|
| OTHER | Dose adjustment of Enoxaparin in patients with sub-therapuetic (prophylactic) levels of factor 10a | We 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.