跳至主要内容
临床试验/EUCTR2008-008723-15-SE
EUCTR2008-008723-15-SE进行中(未招募)不适用

Postoperative Pain Relief following Total Hip Arthroplasty. A comparison between Intrathecal morphine (IM) and Local Infiltration Analgesia (LIA).

Örebro University Hospital0 个研究点开始时间: 2009年3月4日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.50 - 85 year-old undergoing total hip arthroplasty.
  • 2.ASA I – II.
  • 3.Have signed and dated Informed Consent.
  • 4.Willing and able to comply with the protocol for the duration of the trial.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Re-operation of a previous total hip arthroplasty.
  • 2.Allergy/intolerance to local anaesthetics, Morphine, Adrenaline, Ketorolac or Ropivacaine.
  • 3.Serious liver- or renal disease judged by the investigator to be of such dignity as to prevent inclusion into the study.
  • 4.Serious heart disease judged by the investigator to be of such dignity as to prevent inclusion into the study,
  • 5.Patients with chronic pain who are taking opiate analgesics regularly.
  • 6.Major bleeding disorders
  • 7.Chronic obstructive pulmonary disease (COPD)
  • 8.Severe asthma that is difficult to treat
  • 9.Limited breathing capacity due to muscular dystrophy
  • 10.Sleep apnoea syndrome
  • 11.Other contraindication to spinal anaesthesia such as spinal stenosis, local infection or contraindications to local anaesthetics.
  • 12.Participation in another clinical medicinal trial during the last 30 days or where follow-up is not completed.

研究者

发起方
Örebro University Hospital

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