ACTRN12619001168145尚未招募3 期
Randomised control trial assessing impact of 24-hr post-operative lidocaine infusion vs placebo on return of gastrointestinal function in adults undergoing elective laparoscopic colorectal resections.
Dr Rebecca Shine0 个研究点目标入组 60 人开始时间: 2019年8月20日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
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 o limit（—）
- 性别
- All
入选标准
- •INCLUSION CRITERIA
- •All patients >18 years undergoing elective laparoscopic/hybrid colorectal resections for benign or malignant conditions at Austin hospital during the study period.
排除标准
- •Contraindications to IV lidocaine:
- •Known history of allergy or hypersensitivity to Lidocaine (lignocaine) or other amide-type local anaesthetic.
- •Stokes-Adams syndrome or any type of heart block or other high-risk arrhythmias.
- •Severe shock
- •Myasthenia gravis
- •Serious diseases of the CNS or of the spinal cord
- •Other exclusion criteria:
- •Childs Pugh A or worse liver disease
- •CKD with eGFR <40ml/hr
- •Chronic use of opioid analgesia or local anesthetics
- •Patients will be excluded if they were unable to participate in postoperative assessments because of language difficulty, postoperative confusion, or cognitive impairment.
研究者
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