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临床试验/NCT03855969
NCT03855969已完成不适用

Frequency of Central Venous Port Catheter Removal Due to Suspected Infection in Patients Diagnosed With Cancer at a Single Institution: A Retrospective Study.

General Hospital Groeninge1 个研究点 分布在 1 个国家目标入组 1,402 人开始时间: 2019年3月1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
1,402
试验地点
1
主要终点
Suspected infection rate

研究概览

简要总结

Background:

Central venous catheters are frequently used during cancer treatment with the aim of venepreservation. It can facilitate venous access for the safe administration of irritating or vesicant intravenous cancer medications and / or other fluids, to collect blood samples or to ensure accurate venous access for contrast during medical imaging. In addition, this means more comfort for the patient who needs to be punctured less peripherally. However, central venous catheters can also be a source of bloodstream infections and other complications, leading to increased morbidity and hospital costs (1). In our hospital, there is a general practice that if an infection of the device is suspected, the central venous catheter should be removed if antibiotics do not seem or prove to be effective.

The objective of this trial is to assess the frequency of implanted port catheter-removal in cancer patients due to suspected infection of the device in a particular oncology center over a time period of seven years. Furthermore, evidence for real device infections (per/post-surgery) and the potential contribution of different (institution-specific) risk factors on device infection will be explored. There will be focused on implanted port catheters only, as this is the main used central venous access device within the oncological population.

Trial objectives:

The primary aim of this retrospective descriptive trial is to evaluate the frequency of implanted port catheter-removal in cancer patients due to suspected infection of the device, over a time period of seven years.

The secondary aim is to examine whether the device infection could be confirmed during or after removal of the device.

At last, the tertiary aim is to verify whether certain variables can be denoted as potential risk factors for central venous access infection. Selection of those variables of interest will be based on a thorough review of the literature and discussion with the responsible healthcare professionals.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Central venous access device removal in our general hospital
  • •Cancer patient

排除标准

  • 未提供

结局指标

主要结局

Suspected infection rate

时间窗: 2012-2017

How many central venous access devices are removed due to a suspected infection of the device in cancer patients.

次要结局

  • Risk factors for central venous access device infections in cancer patients(2012-2017)
  • Approved infection rate(2012-2017)

研究者

发起方
General Hospital Groeninge
申办方类型
Other
责任方
Principal Investigator
主要研究者

Koen Van Eygen

Principle Investigator

General Hospital Groeninge

研究点 (1)

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