Colorectal Disorders Clinical Trial
Official title:
The Effect of Intraperitoneal Local Anaesthetic on Functional Recovery Following Bowel Resection: A Prospective Randomised Blinded Trial
This study will evaluate the addition of a local anaesthetic infusion into the abdomen to patient controlled analgesia in the management of postoperative pain and recovery after bowel surgery. Half of the patients will have an infusion of a local anaesthetic called ropivacaine and half will have an infusion of placebo in addition to their normal pain relief.
The purpose of this randomised controlled blinded trial is to determine the effectiveness in
every day practice of intraperitoneal local anaesthetic (IPLA) infusion on postoperative
recovery following bowel resection in an optimised Enhanced Recovery After Surgery (ERAS)
setting.
The investigators hypothesise that, in an optimised ERAS setting, intraperitoneal
instillation and infusion of the local anaesthetic ropivacaine to the site of maximal
visceral dissection for 48 hrs will result in an improved functional postoperative recovery
following both open and laparoscopic bowel surgery.
This research will provide evidence to allow recommendation on the routine inclusion of IPLA
into the multimodal analgesia component of ERAS programs for bowel surgery.
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