EUCTR2007-000026-44-DK进行中（未招募）1 期
Hydroxyethylstarch induced coagulopathy and haemostatic potential of fibrinogen - in vivo placebo controlled clinical trial.
Aarhus Universityhospital0 个研究点目标入组 20 人开始时间: 2007年3月28日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 20
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
- •Indication for cystektomia
- •Written informed consent
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Anticoagulant treatment and use of acetylsalicyclic acid and/or NSAID within 2 days.
- •Abnormale preoperative coagulationsparametres (Thr, PP, APTT, D-dimer, Fibrinogen, AT, TT)
- •Disseminated cancer and/or metastasis
- •Amnestic informations or records on schaemic heart disease, claudicatio, universel arteriosklerosis
- •Amnestic informations on familar and/or previous tromboembolic event
- •Renal failure defined as clinical relevant abnomal levels of creatinine
- •Liver failure defined as clinical relevant abnomal levels of ALAT
- •Hypersensibility to Voluven, Haemocomplettan eller ingredient substances
- •Fertile women not using contraception (contraceptive pill, diaphragm, condom)
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