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临床试验/ISRCTN81223298
ISRCTN81223298已完成未知

A randomised controlled trial of thoracic epidural analgesia versus rectus sheath catheters for open midline incisions in major abdominal surgery within an Enhanced Recovery Program

East Lancashire Hospitals NHS Trust (UK)0 个研究点目标入组 132 人开始时间: 2014年1月16日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
132

研究概览

简要总结

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients over 18 years of age
  • 2. Planned elective major abdominal surgery including major colorectal resections, upper GI surgery (e.g. pancreaticoduodectomy) and major urological surgery (e.g. radical cystectomy)
  • 3. Planned open midline surgical incision
  • 4. Included in the ERP
  • 5. Willing and able to give consent
  • 6. American Society of Anesthesiologists (ASA) score 13

排除标准

  • 1. Contraindication to epidural analgesia (e.g. coagulopathy, local infection, systemic sepsis, severe aortic stenosis)
  • 2. Consent refused for either thoracic epidural analgesia (TEA) or Rectus Sheath Catheters (RSCs)
  • 3. Non-English speaker
  • 4. Ano-rectal excision (e.g. pan-proctocolectomy or AP resection)
  • 5. Planned transverse or oblique incisional approach
  • 6. Allergy to local anaesthetic drugs or opiates
  • 7. Opiate tolerance
  • 8. Pre-existing chronic abdominal pain
  • 9. Extensive existing midline abdominal scarring

研究者

发起方
East Lancashire Hospitals NHS Trust (UK)

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