EUCTR2012-002816-19-NL进行中（未招募）不适用
Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous injection of 5700 IU nadroparin in morbidly obese patients after bariatric surgery. - Nadroparin and anti-Xa actitivity after bariatric surgery
Rijnstate Hospital0 个研究点开始时间: 2012年7月3日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •approval for Roux-en-Y gastric bypass
- •total body weight > 140 kg
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 50
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •renal impairment (GFR < 30ml/min and/ or serum creatinin > 150 micromol/ml)
- •Coagulation disorders (APTT/PT > 2x norm)
- •Use of vitamin K antagonists (such as acenocoumarol)
研究者
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Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous administration of 5700 IU nadroparin in morbidly obese patients after bariatric surgery.antistolling profylaxe bij bariatrische chirurgiemorbid obesityprofylaxis thrombosisNL-OMON37098Rijnstate Ziekenhuis50
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