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临床试验/ISRCTN28558391
ISRCTN28558391已完成未知

Post operative pain control after abdominal gynaecological surgery using pump-releasing local anaesthetic for 24 hours continuously: a prospective, double-blind, randomised, placebo-controlled study

Department of Health0 个研究点目标入组 80 人开始时间: 2004年9月30日最近更新:

试验速览

阶段
未知
状态
已完成
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

入排标准

性别
Female

入选标准

  • 80 women aged 30 to 70 years undergoing elective gynaecological surgery performed through a transverse incision in the lower abdomen.

排除标准

  • 1. Patients with a known allergy to morphine, fentanyl, propofol, vecuronium, diclofenac or marcain.
  • 2. Regular medication with opioids for the last 6 months.
  • 3. Body mass index (BMI) greater or equal to 32.
  • 4. Previous major surgery during the last 6 months.

研究者

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