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临床试验/CTRI/2021/12/038632
CTRI/2021/12/038632已完成不适用

SURGICAL SITE INFECTION FOLLOWING WOUND IRRIGATION WITH POVIDONE-IODINE VS NORMAL SALINE BEFORE SKIN CLOSURE IN CAESAREAN SECTIONS

PGIMER Chandigarh1 个研究点 分布在 1 个国家目标入组 476 人开始时间: 2021年12月15日最近更新:
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试验速览

阶段
不适用
状态
已完成
入组人数
476
试验地点
1
主要终点
to study incidence of SSI in elective and emergency caesarean section undergoing wound irrigation with povidone-iodine or normal saline
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

To assess the incidence of SSI in women following wound irrigation with povidone iodine vs normal saline before skin closure in caesarean sections

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Participant and Investigator Blinded

入排标准

年龄范围
15.00 Year(s) 至 49.00 Year(s)（—）
性别
Female

入选标准

  • •All emergency and elective caesarean sections.

排除标准

  • •on immunosuppressant drugs suspected or known allergy to iodine class III or class IV wound.

结局指标

主要结局

to study incidence of SSI in elective and emergency caesarean section undergoing wound irrigation with povidone-iodine or normal saline

时间窗: to study incidence of SSI in elective and emergency caesarean section undergoing wound irrigation with povidone-iodine or normal saline | assessment for SSI will be done at day 7 post op, 2 weeks and 4 weeks

次要结局

  • to study incidence of culture positive SSI in elective and emergency caesarean section(to measure incidence of specific organism cultured in SSI in elective and emergency caesarean)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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