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临床试验/PACTR202303749998721
PACTR202303749998721已完成Unknown

Comparison of immediate and early oral feeding regimens following uncomplicated caesarean sections in Ile-Ife, Nigeria: a randomized controlled trial

Akaninyene Ubom0 个研究点目标入组 162 人开始时间: 2023年3月6日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
162

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

  • All consenting pregnant women who undergo elective and emergency uncomplicated caesarean sections under regional anesthesia (spinal, epidural and combined spinal-epidural) will be recruited for the study.

排除标准

  • 1. Caesarean sections involving bladder, ureteral, intestinal or uterine artery injury
  • 2. Caesarean sections involving blood loss >1,000 ml
  • 3. Caesarean sections involving extensive adhesions/adhesiolysis or/and extensive bowel handling
  • 4. Caesarean sections performed under general anaesthesia
  • 5. Patients with prolonged obstructed labour or obstructed labour with features suggestive of sepsis or/and peritonitis
  • 6.Patients with severe and uncontrolled medical conditions eg diabetes mellitus, preeclampsia/eclampsia, chronic kidney and liver disease or/and requiring intensive care
  • 7. Chronic gastrointestinal disorders such as chronic constipation, irritable bowel syndrome, malabsorption disorders

研究者

发起方
Akaninyene Ubom

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