JPRN-UMIN000005333已完成3 期
A Randomized Controlled Trial of Enoxaparin Combined with Intermittent Pneumatic Compression versus Intermittent Pneumatic Compression Alone as Prophylaxis against Thromboembolism in Postoperative Gynecologic Oncology Patients - RCT of Combined Enoxaparin/IPC vs. IPC Alone in Postoperative Gynecologic Oncology Patients
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 40years-old 至 ot applicable（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •Patients with venous thromboembolism Patients allergic to enoxaparin and/or heparin/heparin derivatives Patients with active bleeding (intracranial hemorrhage, retroperitoneal hemorrhage, and/or hemorrhage from other major organs) or at higher risk of bleeding (hemostatic disorder, gastric ulcer, recent ischemic stroke, uncontrollable hypertension, diabetic retinopathy, and/or recent brain or eye surgery) Patients with acute bacterial endocarditis Patients with severe renal dysfunction (CCr < 50ml/min = eGFR < 40ml/min/1.73m2) Patients with severe liver dysfunction Patients with history of heparin induced thrombocytopenia (HIT) Patients with history of venous thromboembolism and/or thrombotic tendency Patients taking anticoagulants, platelet aggregation inhibitors, salicylic acid derivatives, and/or thrombolytic drugs
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