跳至主要内容
临床试验/NCT00549705
NCT00549705已完成不适用

Registry of Hospitalized Patients Treated With Fondaparinux

Brigham and Women's Hospital0 个研究点目标入组 220 人开始时间: 2007年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
220
主要终点
Venous Thromboembolism and Bleeding Events

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • BWH hospitalized patients receiving Fondaparinux

排除标准

  • 未提供

结局指标

主要结局

Venous Thromboembolism and Bleeding Events

时间窗: 90 Days

次要结局

  • Mortality(30 Days)

研究者

申办方类型
Other

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