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临床试验/ACTRN12620000714987
ACTRN12620000714987尚未招募未知

Comparison of recovery after surgery between opioid and opioid-free anaesthesia for elective laparoscopic abdominal surgery

Wide Bay Hospital and Health Service0 个研究点目标入组 80 人开始时间: 2020年7月1日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
80

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
Blinded (masking used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Patients may be included in the study only if they meet all of the following criteria:
  • Aged 18 - 65 years
  • Independent capacity to consent to participate in trial
  • American Society of Anaesthesiologists (ASA) physical health score of I - II
  • Booked for elective laparoscopic cholecystectomy or tubal ligation (with or without oophorectomy)

排除标准

  • Patients who fulfil any of the following criteria are not eligible for admission to the study:
  • Pregnant women
  • Body Mass Index > 35
  • Allergy to opioids
  • Allergy to adjuvant drugs
  • Persistent opioid use - patients with Oral Morphine Equivalent Daily Dose (OMEDD) greater than 0 during previous week pre-op and taken for 7 successive days or more including recreational drug use.
  • Non-elective surgery

研究者

发起方
Wide Bay Hospital and Health Service

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