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临床试验/NCT03875352
NCT03875352已完成不适用

The Influence of Nursing Technique Applied at the Central Venous Catheter Insertion Site Upon the Incidence of Infection

University Hospital Ostrava2 个研究点 分布在 1 个国家目标入组 221 人开始时间: 2016年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
221
试验地点
2
主要终点
Local signs of inflammation

研究概览

简要总结

Assessing the impact of the nursing technique applied at the insertion site of the central venous catheter using hydrophilic methacrylate gel (HMG) and 2% Chlorhexidine (CHG) upon the incidence of inflammatory complications when treating the surrounding of the central venous catheter.

详细描述

The study was a prospective and randomized clinical trial. The study was performed at two departments of the University Hospital Ostrava.

The design and performance of the study were approved by the Ethics Committee of the University Hospital Ostrava.

The patients indicated for insertion of central venous catheter (CVC) were informed about the possible nursing techniques applied at the insertion site of the central venous catheter, participation in the study was conditioned with signing a written informed consent. The study evaluated the superiority of a new procedure in providing nursing care for patients with CVC.

Basic patient characteristics were observed and recorded according to the protocol of the study (age, sex, diagnosis), the number of days with CVC inserted, type of dressing, APACHE II score, the presence of neutropenia and the final score of assessment of local signs of inflammation, which was defined as follows:

0 points = No reddening

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

盲法说明

The study was designed as open-label, no masking was used in the protocol.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age over 18 years
  • Patients with CVC
  • Hospitalization at ICU

排除标准

  • Allergy to HMG
  • Allergy to transparent foil
  • CVC insertion shorter than 3 days
  • Strong bleeding from CVC insertion site

研究组 & 干预措施

Neutropenia patients

Experimental

Patients with neutropenia were treated using the CHG and HMG technique.

干预措施: CHG technique (Procedure)

Neutropenia patients

Experimental

Patients with neutropenia were treated using the CHG and HMG technique.

干预措施: HMG technique (Procedure)

No neutropenia patients

Experimental

Patients with no neutropenia were treated using the CHG and HMG technique.

干预措施: CHG technique (Procedure)

No neutropenia patients

Experimental

Patients with no neutropenia were treated using the CHG and HMG technique.

干预措施: HMG technique (Procedure)

结局指标

主要结局

Local signs of inflammation

时间窗: 3 days at minimum, up to 15 days

The local signs of inflammation were observed in both study arms and both interventions, and were assessed according to the scoring system described in detail description.

次要结局

未报告次要终点

研究者

发起方
University Hospital Ostrava
申办方类型
Other
责任方
Sponsor

研究点 (2)

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