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临床试验/NCT07600463
NCT07600463尚未招募不适用

UVC in Prevention of Surgical Wound Infection

Ville Leinonen1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2026年6月4日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
75
试验地点
1

研究概览

简要总结

The LF-PODD study investigates the use of UVC (270nm) light in the prevention of surgical wound infections. Three devices are used in the study, two of which are actively producing UVC light (265 and 275 nm) and one device does not produce UVC light at all. The devices are outwardly completely identical and the devices are drawn for the research participants. Volunteers for neurosurgical procedures are selected for the study. Everyone participating in the study will be informed about the research and written consent will be requested. In the study, UVC light is focused on the surgical area at the beginning of the neurosurgical operation, during the operation, the device automatically dispenses UVC light into the air of the surgical area every 20 minutes, and at the end of the surgical procedure, the device delivers a single dose of UVC light to the surgical wound after closing the surgical wound. Study participants are monitored according to the standard treatment protocol and, in particular, the inflammation of the surgical wound is monitored. The results of the study are recorded and analysed using statistical methods.

详细描述

The following are recruited for the study:

75 patients undergoing elective CSF shunt surgeries

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • 75 patients with idiopathic normal pressure hydrocephalus (iNPH) arriving for CSF shunt procedure
  • written informed consent

排除标准

  • immunosupressive medication
  • pregnancy
  • medication sensitizing for light exposure (e.g. doxycycline)

研究者

发起方
Ville Leinonen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ville Leinonen

Professor

Kuopio University Hospital

研究点 (1)

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