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临床试验/ISRCTN15475290
ISRCTN15475290进行中(未招募)未知

CAMELOT - Continuous rectus sheath Analgesia in eMErgency LaparOTomy. A Multi-centre, randomised sham-controlled trial of rectus sheath catheter-delivered local anaesthetic infusion compared with usual care in patients undergoing emergency bowel surgery.

niversity Hospital Southampton NHS Foundation Trust0 个研究点目标入组 750 人开始时间: 2022年8月9日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
750

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
All

入选标准

  • 1. Aged =18 years
  • 2. Undergoing emergency laparotomy surgery via a midline incision
  • 3. Eligible for inclusion in the National Emergency Laparotomy Audit (NELA)

排除标准

  • Current participant exclusion criteria:
  • 1. Planned epidural anaesthesia
  • 2. Clinician refusal
  • 3. Lack of mental capacity to consent to trial participation
  • 4. Contraindications to RSC including allergy to local anaesthetic (LA), anatomical factors making RSC insertion impossible
  • 5. Existing co-enrolment in another clinical study if:
  • 5.1. The intervention in the other study is expected to influence the primary outcome (this will be considered by a senior clinician on a case-by-case basis)
  • 5.2. It is considered too burdensome for the patient; or
  • 5.3. It is not permitted by the other study
  • 6. Previous enrolment in the CAMELOT trial
  • Previous participant exclusion criteria:
  • 1. Clinician or patient refusal to participate
  • 2. Planned epidural anaesthesia
  • 3. Contraindications to Rectus Sheath Catheter (RSC) including allergy to local anaesthetic (LA)
  • 4. Anatomical factors making RSC insertion impossible

研究者

发起方
niversity Hospital Southampton NHS Foundation Trust

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