NCT00535171已完成不适用
Venous Thromboembolism Taskforce Audit Program
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Sanofi
- 入组人数
- 8,764
- 试验地点
- 1
研究概览
简要总结
To determine the effect of an interventional campaign run by a dedicated "VTE Nurse Educator" over a 6-month period and the effect on prophylaxis rates.
To determine the proportion of medically admitted patients with risk factors for VTE.
To assess and compare the use of venous thromboembolism (VTE) prophylaxis in hospitalized medical patients versus recommendations and current guidelines.
To determine the patient characteristics of those deemed to be at risk of VTE. To determine the proportion of patients receiving appropriate thromboprophylaxis for their risk.
To determine the type and duration (where possible) of prophylaxis used.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Hospital admission for an acute illness with an in-patient hospital stay of 3 days or more.
排除标准
- •Patients who have undergone any type of surgery during current admission
- •Patients who are admitted to a ward or department that is excluded from this study e.g psychiatric, paediatric, maternity, intensive care unit, coronary care unit.
- •Prior enrollment in this protocol during current admission
- •Prior enrollment in a VTE study involving pharmaceutical or mechanical treatment within last 90 days.
- •Admission for suspected or diagnosed deep vein thrombosis
- •The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
研究者
研究点 (1)
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