跳至主要内容
临床试验/DRKS00029941
DRKS00029941已完成不适用

Optimisation of intermittent pneumatic compression in patients with oedema of the legs of different etiologies - IPC+ trial

Bauerfeind AG - Phlebology Business Development & Medical Affairs0 个研究点目标入组 18 人开始时间: 2022年8月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
18

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Oedema of the legs: primary and secondary lymphoedema, phleboedema, lipoedema.
  • Willingness and ability of the patient to apply intermittent pneumatic compression and to wear multi-layer compression bandages, and to follow the instructions of the doctor and the staff
  • Age between = 18 years
  • Presentation of the written declaration of consent to participate in the observational study after detailed information about the nature, significance, risks and scope of the observational study as well as about the expected desired and undesired effects of the treatment in the context of the observational study.
  • Sufficient written and spoken German language skills

排除标准

  • Acute deep venous thrombosis and acute thrombophlebitis
  • Peripheral arterial occlusive disease stage III and IV according to Fontaine
  • Decompensated heart failure and severe, non-adjustable arterial hypertension (diastolic > 100 mmHg)
  • Acute tissue trauma, acute erysipelas (with systemic signs such as fever, reduced general condition, signs of sepsis)

研究者

发起方
Bauerfeind AG - Phlebology Business Development & Medical Affairs

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