Antiseptic Washing Prior to Skin Closure During Cesarean Delivery- a Randomized Control Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 600
- 试验地点
- 1
- 主要终点
- surgical site infection
研究概览
简要总结
The goal of this clinical trial is to learn if antiseptic washing prior to skin closure during cesarean section reduces rates of surgical site infection.
intraoperative washing is a common practice in other surgical fields and several studies have shown efficacy in reducing postoperative infection rates. no randomized control trial has tested this intervention during cesarean section.
The main questions we aim to answer are:
Does subcutaneous antiseptic washing reduce the rates of surgical site infection? Does antiseptic washing improve scar healing? Does antiseptic washing reduce hospital stay, postpartum fever rates and readmission cases?
Researchers will compare subcutaneous antiseptic washing to no intervention to see if surgical site infection rates reduce
Participants will:
consent to participate in the trial Visit the postpartum clinic 30 days after surgery
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •pregnant women undergoing cesarean delivery
排除标准
- •pregnant women undergoing vaginal delivery
研究组 & 干预措施
Subcutan lavage
Subcutaneous washing with antiseptic solution: Chlorhexidine gluconate 0.2%
干预措施: Subcutaneous washing (Procedure)
no lavage
No subcutaneous washing
干预措施: no subcutaneous washing (Procedure)
结局指标
主要结局
surgical site infection
时间窗: 30 days after surgery
SSI infection rates
次要结局
- postpartum fever(30 days after surgery)
- wound healing(30 days after surgery)
- hospital stay(30 days after surgery)