A multimodal, adaptive, intervention to prevent perioperative infection and reduce mortality: a stepped-wedge cluster RCT (The Modified Clean Cut Trial)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 980
- 试验地点
- 10
- 主要终点
- Primary outcomes include Surgical Site Infections (SSIs) up to 30 days
研究概览
简要总结
A multimodal, adaptive, intervention to prevent perioperative infection and reduce mortality: a
stepped-wedge cluster RCT (The Modified Clean Cut Trial)
The purpose of Clean Cut is to:
(1) help facilitate improved adherence to critical perioperative infection prevention practices
and lower surgical site infection rates; postoperative morbidity and mortality.
(2) create an environment conducive to successful implementation of the WHO Surgical Safety
Checklist;
(3) foster a culture of teamwork, individual value, and accountability that facilitates quality
improvement more broadly.
Research questions: Does a surgical infection prevention programme intervention lead to a reduction in surgical infections and postoperative mortality? Can we increase adherence to critical standards of perioperative care in a sustainable manner?
What are the barriers and facilitators to compliance with perioperative standards? Is a strategy of peer-to-peer learning and hub-and-spoke support adequate for effective implementation?
Study design and sample size: Stepped wedge, mixed methods, team-based intervention to improve compliance with seven critical perioperative infection prevention standards in 900 patients undergoing abdominal surgery.
Intervention: Clean Cut has been developed through a collaboration informed and led by
LMIC healthcare staff. Further modifications to this intervention have been added to this by the India Hub of the NIHR Health Research Unit On Global Surgery following our work especially in the Cheetah Trial. It involves a sequential intervention to address problems in adhering to seven critical standards of perioperative infection prevention and control:
- Appropriate skin preparation of both the surgeon’s hands and the surgical site with proper
antiseptic agents
- Maintenance of the sterile field by ensuring the integrity and sterility of surgical gowns,
drapes, and gloves.
- Appropriate antibiotic selection and administration, when indicated, within one hour prior
to surgical incision to optimise prophylaxis
-
Proper confirmation of instrument sterility by the operating team
-
Complete gauze/swab counts every case at appropriate times (preoperatively, before organ
space and/or cavity closure, and postoperatively)
- Change of Gloves and Instruments by the Surgical Team at the time of Fascial Closure in
Contaminated and Dirty Abdominal Operations.
- Use of the Surgical Safety Checklist to promote teamwork, communication, and a culture
of safety in the operating room
The qualitative part of the study will involve a validated patient safety questionnaire administered to perioperative personnel and surgeons. A semi structured interview and focussed group discussions will also be conducted to identify barriers to teamwork and patient safety in the operating room and find solutions.
Duration: 36 months
Statistical Analysis Plan: Key variables including compliance with perioperative standards and
patient outcomes will be measured using standardized tools and assessments. Data will be
collected using electronic data capture systems and analyzed using appropriate statistical
methods, including regression analysis to evaluate the intervention’s impact on primary and
secondary outcomes. Data will be summarized using frequency distribution and descriptive
analysis. The normality of the data will be assessed through the statistical test and graphical
method. The p-value of 0.05 will be considered as statistically significant. Summary statistics
will be presented for all outcome measures, with the relevant adjusted effect measures, 95%
confidence intervals and p-values from two-sided tests. The adjusted model will include hospital
as fixed effects and centre as a random effect to account for the clustered nature of the sample.
Quantitative data will be analyzed using statistical software such as R or SPSS, while qualitative
data will be analyzed thematically.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 0.00 Day(s) 至 99.00 Year(s)(—)
- 性别
- All
入选标准
- •Patient undergoing any abdominal surgery (including the abdominal wall or entering the abdominal or retroperitoneal cavities)
- •Any age, gender of patient
- •Ability to complete postoperative 30 day follow up.
排除标准
- •Surgery in any part of the body other than abdomen
- •Patient unable to complete postoperative 30 day follow-up.
结局指标
主要结局
Primary outcomes include Surgical Site Infections (SSIs) up to 30 days
时间窗: Primary outcomes include Surgical Site Infections (SSIs) up to 30 days | of surgery
of surgery
时间窗: Primary outcomes include Surgical Site Infections (SSIs) up to 30 days | of surgery
次要结局
- Secondary outcomes include all cause mortality , length of stay, reoperation for any reason((planned or unplanned), and overall compliance with the seven perioperative infection)
研究者
Dr Amit Mahajan
Christian Medical College & Hospital Ludhiana
