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临床试验/NCT06420934
NCT06420934招募中不适用

Comparison of the Breach of the Aseptic Barrier After Surgical Handwashing: Drying With One or Two Surgical Towels

Instituto de Ortopedia Infantil Roosevelt2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2024年4月26日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
72
试验地点
2
主要终点
Contamination

研究概览

简要总结

This study aims to determine whether the use of two sterile towels for drying after surgical handwashing results in fewer contamination events compared to the use of only one towel among healthcare personnel. This randomized, multicenter, superiority-controlled trial will enroll up to 72 healthcare workers and surgical residents from three hospitals in Bogotá, Colombia. A fluorescent product will simulate bacteria, and contamination will be assessed by evaluating the presence of fluorescent cream after hand drying technique with either two or one surgical sterile towel. Data will be collected through REDCap and deidentified. Differences in the proportion of contamination between the two groups will be assessed using an exact Fischer test, and confounding variables will be included in the analysis through logistic multivariate regression, with a significance level set a priori at 0.05. Results will be submitted for publication in a peer-reviewed journal.

详细描述

Approval was obtained from the ethics committee of three healthcare institutions. A process of informed consent will be conducted with all participants, and confidentiality and data protection will be guaranteed. A research assistant, unaware of the operational hypotheses and study objectives, will execute the experiment and record the results. There will be no blinding of the intervention for the participants or the assistant. At each institution, randomization will be conducted a priori to determine the operating room where participants should be recruited. Likewise, the intervention to be administered will be randomized. All these data will be stored in opaque envelopes that will be opened at the time of recruitment. A total of 72 participants will be recruited, with 36 exposed to drying with one towel and 36 to drying with two towels. Recruitment will cease upon completion of the respective participants stipulated for each intervention.

The primary outcome of interest will be the presence or absence of contamination. To evaluate this outcome, the gold standard would be the collection of cultures and the analysis of the presence or absence of bacterial contamination. However, due to the costs and methodological difficulties of taking cultures, an indirect method, previously validated as a surrogate, will be employed instead. 2 mL of fluorescent cream (Glo Germ ™) will be applied with a brush proximal to the normally washed area during surgical scrubbing (3 cm above the elbow). Participants will be shown a video on how to dry with one or two surgical towels and will be given one minute to do so. Subsequently, the presence or absence of fluorescent cream on the upper extremities will be evaluated using a UV light lamp. If fluorescence is evidenced in the washed area where it was not applied, it will be considered that there was contamination during the hand drying process.

No interim analyses will be executed. Data will be de-identified for the analysis. Descriptive statistics will be conducted using R studio, and proportions of contamination when drying with one or two towels will be compared. A simple logistic regression will be performed to assess the relationship between the intervention and the proportion of contamination events, and a multivariate logistic regression will be conducted to assess the effect of confounding variables on the outcome. The results will be reported collectively for publication in a peer-reviewed journal.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Masking will be provided to data analysis expert.

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

  • Workers and students who have a current affiliation with the institutions where the study will be executed.
  • Workers and students whose practice or work involves performing surgical handwashing at least once a week for invasive procedures.

排除标准

  • Workers and students who do not wish to participate in the study.
  • Workers and students whose work activities do not allow them time to participate in the study.
  • Workers and students who are allergic to the fluorescent cream
  • Workers and students whose nails exceed a length of 0.5 cm from the fingertip edge.
  • Workers and students whose nails are painted with polish.
  • Workers and students who refuse to remove jewelry and accessories from wrists and hands.
  • Workers and students with recent wounds on hands or forearms, including tattoos done in the last month.
  • Workers and students who do not adhere to the handwashing and drying technique taught prior to the study's implementation.

结局指标

主要结局

Contamination

时间窗: 3 minutes after handwash and hand drying.

Presence or absence of fluorescent cream on the upper extremities will be evaluated using a UV light lamp in a dark room. If fluorescence is observed in the washed area where it was not applied, it will be considered that there was contamination during the hand drying process.

次要结局

未报告次要终点

研究者

发起方
Instituto de Ortopedia Infantil Roosevelt
申办方类型
Other
责任方
Sponsor

研究点 (2)

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