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临床试验/PACTR202308689414142
PACTR202308689414142招募中Unknown

Effect of preoperative vaginal preparation with 0.3% chlorhexidine-cetrimide versus 10% povidone-iodine on post cesarean section infection.

OHIOMOBA GLADYS0 个研究点目标入组 250 人开始时间: 2023年7月21日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Ages eligible for study: =18 years
  • - All pregnant women with gestational age of 28 weeks and above.
  • - Pregnant women with indication for emergency or elective Cesarean section.
  • - Patient must give informed consent.

排除标准

  • -Allergy/Contraindications to either Povidone-Iodine (thyroid disease) and Chlorhexidine
  • -Obstructed Labour
  • -Active genital herpes
  • -Face Presentation
  • -Antepartum hemorrhage, cord prolapse with life fetus
  • -Active Chorioamnionitis,
  • -Women on chronic steroid use, Diabetes Mellitus, HIV infection,
  • -Intrauterine Fetal Death
  • -Evidence of pre-operative skin infection
  • -Women considered for a hysterectomy at the time a decision for Cesarean section was made were also excluded.

研究者

发起方
OHIOMOBA GLADYS

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