跳至主要内容
临床试验/NL-OMON36555
NL-OMON36555已完成不适用

Exploring alternative wound care treatment for percutanous gastrostomy site infection: a prospective, randomized, open, blinded end-point (PROBE) design. - PEG-protocol

Vrije Universiteit Medisch Centrum0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Signed informed consent
  • PEG-site infection graded as type 1 (early signs of inflammation<=proactive measures)
  • & type 2 (requiring local antiseptic/antibiotic care)
  • Male and female participants age 18 and older
  • PEG insertion procedure longer than 1 week prior to randomization
  • Patient or guardian is able to fully comprehend and perform study procedures

排除标准

  • Estimated life expectancy less than one month
  • Concurrent use of oral antibiotics for other diagnosis
  • Signs and symptoms of concurrent disease for which the subject is expected to start antibiotic treatment
  • PEG-site infection graded as type 3 (requiring systemic antibiotics )
  • & 4 (requiring surgery or PEG-tube removal)

研究者

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