ACTRN12615000554561已完成4 期
Do patients undergoing major abdominal surgery benefit from use of the Painbuster rectus sheath infusion device for improving analgesia or reducing opioid requirement in the post-operative period, a double blinded placebo controlled trial.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 110
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 80 Years(—)
- 性别
- All
入选标准
- •Midline laparotomy
- •Planned painbuster device as part of analgesic regimen
排除标准
- •Exclusions would be patient refusal,
- •plan for epidural analgesia and inability to follow up the patient i.e. not able to communicate for any reason (dementia, not able to speak English) and expected ICU admission following surgery.
研究者
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