jRCT1041200056已完成不适用
Randomized controlled trial of surgical wounds antisepsis with aqueous povidone-iodine for prophylaxis of surgical site infection in gastroenterological surgery. (SURPRISE trial)
None0 个研究点目标入组 700 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 700
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Single Blind
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •Intended for patients who meet all of the following criteria:
- •Patients who are over 20 years old when obtaining consent (regardless of gender)
- •Patients undergoing gastroentelogical surgery (such as surgery for esophagus, stomach, small intestine, large intestine, liver, biliary tract, or pancreas) meeting wound class 2, 3, 4) .
- •Patients who have received sufficient explanation for participation in this study, and who have provided written consent.
排除标准
- •Patients who violate any of the following will not be included in this study:
- •Patients who have allergy for popidone iodine.
- •follow-up failure due to pass away or other reasons
- •Patients who hav active infection excluding viral hepatitis
- •Patients who are in pregnancy or may be pregnant.
- •Patients lactating.
- •Patients with sever thyroid dysfunction.
- •Any patients who judged to be inappropriate by the study investigators.
结局指标
主要结局
-
Postoperative 30-day surgical site infection (SSI) rate
次要结局
- Postoperative 30-day allergies events rate(Postoperative 30-day)
研究者
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