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Registry of Hospitalized Patients Treated With Fondaparinux

Registry of Hospitalized Patients Treated With Fondaparinux

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00549705
Enrollment
220
Registered
2007-10-26
Start date
2007-07-31
Completion date
2009-06-30
Last updated
2009-09-17

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

Conditions

Deep Vein Thrombosis, Pulmonary Embolism

Keywords

Anticoagulation, Thrombosis, Bleeding, Clotting, Pulmonary Embolism, Deep Vein Thrombosis

Brief summary

Registry of Hospitalized patients at Brigham and Women's Hospital treated with Fondaparinux

Detailed description

The use of antithrombotic agents in the hospital is the mainstay of therapy for the treatment or prophylaxis of venous thromboembolism (VTE) and acute coronary syndrome (ACS). Concern with the administration of heparins and risk for adverse sequelae has led to the development of newer, longer-acting agents. Fondaparinux offers once daily administration with only an extremely small risk of developing heparin induced thrombocytopenia. Recent data have further demonstrated the efficacy and safety of Fondaparinux in VTE and ACS, expanding its use in clinical practice. We aim to: 1) determine how Fondaparinux is being used in a real life clinical setting, a tertiary-care academic medical center (BWH), and 2) assess the associated clinical outcomes at 90 days after initiation of Fondaparinux.

Interventions

None listed

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* BWH hospitalized patients receiving Fondaparinux

Design outcomes

Primary

MeasureTime frame
Venous Thromboembolism and Bleeding Events90 Days

Secondary

MeasureTime frame
Mortality30 Days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026