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A Comparison of Extended Versus Conventional Duration of Enoxaparin Prophylaxis (i.e., Preventive Treatment) for Venous Thromboembolism (VTE, i.e., Blood Clots in the Veins) and Bleeding Event Risk in a Population With Acute Medical Illness

NCT05819112

TerminatedN/A

Sponsor: Sanofi

Conditions: Venous Thromboembolism

Countries: United States

Venous Thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), is associated with an increase in risk of mortality and long-term disability and is a major contributor to global disease burden. Participants hospitalized with an acute medical illness are at increased risk of VTE. This study a non-interventional study which analyzes data already collected in the Optum US clinical database. Its aim is to compare conventional versus extended duration prophylaxis with enoxaparin on the incidence of VTE and bleeding events in participants hospitalized for acute medical illness. The first date of enoxaparin treatment will be the index date.

Eligibility overview

Sex: ALL

Age: 40 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Hospitalization for the following acute conditions:

  * Infection
  * Respiratory insufficiency
  * Inflammatory condition
  * Cancer
  * Heart failure
  * Ischemic stroke
* Initiation of enoxaparin prophylaxis during hospitalization (index date)
* Age ≥40 years

Exclusion Criteria:

* Symptomatic VTE or major bleeding event 90-days prior to index date
* Major surgery within (+1,-90) days from index date
* Ongoing anticoagulation therapy (medication supply within \[-2,-32\] days from index date)
* Atrial fibrillation
* Chronic kidney disease (CKD) stages IV and V, or dialysis

The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.

Locations (1)

Bridgewater, New Jersey, United States