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Rate of Venous Thrombosis in Acutely Ill Patients Hospitalized in Internal Medicine Wards

Rate of Venous Thrombosis in Acutely Ill Patients Hospitalized in Internal Medicine Wards

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03157843
Acronym
AURELIO
Enrollment
1000
Registered
2017-05-17
Start date
2015-02-28
Completion date
2018-01-31
Last updated
2017-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Venous Thromboembolism, Deep Venous Thrombosis

Brief summary

After reports from observational studies suggesting an association between acutely ill medical patients and venous thromboembolism (VTE), interventional trials with anticoagulants drugs have demonstrated a significant reduction of VTE during and immediately after hospitalisation. Although several guidelines suggest the clinical relevance of reducing this outcome, there is a low tendency to use anticoagulants in patients hospitalised for acute medical illness. This observational multicentre study wants to evaluate the incidence of venous thrombo-embolism in acutely ill patients hospitalized in internal medicine wards.

Detailed description

Epidemiological studies have provided evidence of a high rate of thromboembolism in patients hospitalised in medical wards. Based on this, several clinical trials with anticoagulants including low-molecular-weight heparin (LMWH) and fondaparinux have been performed in patients hospitalised for acute medical illness to prevent thromboembolism. Interventional trials consistently showed that prophylaxis with anticoagulants reduces the risk of composite endpoints of deep venous thrombosis (DVT), pulmonary embolism (PE) and DVT-related death. These results prompted recommendation to the use anticoagulant prophylaxis in patients hospitalised for acute medical illness, but, despite this, there is a widespread underuse of anticoagulant prophylaxis in the medical wards of hospitals. This observational multicentre study wants to evaluate the incidence of venous thrombo-embolism in acutely ill patients hospitalized in internal medicine wards.

Interventions

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* pneumonia * heart failure * Chronic Obstructive Pulmonary Disease * Kidney failure * syncope * atrial fibrillation * Urinary Tract Infection * Anemia * arthritis * Diabetic Ketoacidosis * unstable angina * asthma * cirrhosis

Exclusion criteria

* treatment with vitamin k inhibitors * surgical interventions * deep venous thrombosis * pulmonary embolism

Design outcomes

Primary

MeasureTime frameDescription
Venous thrombo-embolismBaseline, up to 4 weeksEvaluation of deep venous thrombosis by compression ultrasonography (CUS)

Countries

Italy

Contacts

Primary ContactFrancesco Violi, MD
francesco.violi@uniroma1.it064461933
Backup ContactLorenzo Loffredo, MD
lorenzo.loffredo@uniroma1.it0649970103

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026