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临床试验/DRKS00015841
DRKS00015841招募中3 期

Feasibility of a neuromuscular electrostimulation device for mechanical thromboprophylaxis in ICU patients - geko in ICU patients

Medizinische Universität Wien0 个研究点目标入组 100 人开始时间: 2018年11月2日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 110 Years(—)
性别
All

入选标准

  • age = 18 years, Caprini Score = 5 indicating the highest risk of VTE and therefore combined VTE prophylaxis (Enoxaparin 1x40mg + mechanical device)

排除标准

  • patient`s refusal of participation, neuromuscular disorder of the lower limbs, formally prohibition of muscle movement in the lower limb (e.g. after certain surgical procedures), implanted electronic devices (e.g. pacemaker), recently diagnosed or suspected thromboembolic event (especially DVT), local open wound or cancerous lesion, pregnancy, epilepsy

研究者

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