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临床试验/ACTRN12614000601639
ACTRN12614000601639招募中未知

A prospective cohort comparing post-operative opioid requirement and other pain related behaviours and effects after major surgery in two Chinese populations from Hong Kong and Mainland China

Dr Alex Konstantatos0 个研究点目标入组 250 人开始时间: 2014年6月5日最近更新:
适应症

试验速览

阶段
未知
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
Observational

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • Patients are eligible for the study if
  • 1.18 and 80 years
  • 2.undergoing major abdominal surgery requiring a wound incision > 10 cm in length.
  • 3. All patients should have strong Chinese features and lived in their respective cities (Hong Kong or Hangzhou) for most of their lives.

排除标准

  • Patients are excluded if they:
  • 1. do not agree to receive patient controlled analgesia (PCA) with morphine for at least three days after surgery
  • 2. do not demonstrate adequate understanding on the principles involving the use of PCA during the preoperative visit.
  • 3. Allergy to morphine, paracetamol or non-steroidal anti-inflammatory drugs.
  • 4. Patients with pre-existing severe renal and liver disease, 5. chronic pain for > 3 months in the 6 months leading to surgery or who require opioid therapy in the preceding 2 weeks prior to surgery

研究者

发起方
Dr Alex Konstantatos

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