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临床试验/ACTRN12618001419257
ACTRN12618001419257撤回未知

Efficacy of warm humidified insufflation for reducing post-operative ileus in women undergoing open surgery for presumed advanced ovarian, tubal or peritoneal malignancy: A randomised single-blind controlled trial.

Fisher and Paykel Healthcare0 个研究点目标入组 226 人开始时间: 2018年8月24日最近更新:
适应症

试验速览

阶段
未知
状态
撤回
发起方
入组人数
226

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
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • Age 18 or older
  • Consented for Open Debulking surgery for presumed advanced ovarian, tubal or peritoneal malignancy.
  • Primary, Interval (after initial chemotherapy), or recurrent setting
  • Able to give informed consent and understand risks and benefits of the study

排除标准

  • Active inflammatory bowel disease
  • Moderate to severe renal impairment (eGFR<50mL/min/1.73m2)
  • Severe hepatic impairment (Child-Pugh C)
  • Pre-existing gut motility disorder including endocrine, metabolic or neurological cause
  • Pre-operative malnutrition requiring parenteral nutrition
  • Inability to give consent or participate in post-operative assessments due to dementia, cognitive impairment, language difficulties, delirium

研究者

发起方
Fisher and Paykel Healthcare

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