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临床试验/DRKS00017035
DRKS00017035招募中未知

Prospective, open study on postoperative care with kinesiotape under conventional compression therapy vs. conventional compression therapy after a cross- and saphenectomy of the saphenous magna vein or saphenous parva vein with sideastexhairsis.

Venenzentrum der Dermatologischen und Gefäßchirurgischen Kliniken St. Maria Hilf Krankenhaus0 个研究点目标入组 44 人开始时间: 2019年3月27日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
44

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 80 Years(—)
性别
All

入选标准

  • Age between 18 and 80 years
  • - Written consent of the patient
  • - BMI 20-40 kg/qm
  • - Bilateral, similar cross- and saphenectomy plus sideastexhairsis (e.g. VSM or VSP) in the venous centre of the Dermatological and Vascular Surgery Clinics, RUB
  • - Inpatient therapy of the patient
  • - Conventional compression stocking treatment after surgery (MKS AG II or MKS AT II)
  • - Physical and mental ability of the patient to record and answer the questionnaire

排除标准

  • - absence of consent of the patient
  • - severe concomitant diseases which have a considerable influence on the target parameters - e.g. unilateral lymphedema
  • - skin diseases that do not allow the tape to be attached to the target leg (e.g. atopic eczema)
  • - Known incompatibility to kinesiotape (cotton / acrylate adhesive)
  • - Inadequate compliance/ possibility to participate in the inspection appointments
  • - Patient wants a different kind of postoperative care.

研究者

发起方
Venenzentrum der Dermatologischen und Gefäßchirurgischen Kliniken St. Maria Hilf Krankenhaus

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