ISRCTN29594895进行中（未招募）未知
A randomised feasibility study evaluating the effect of perioperative intravenous lIdocaine on colorectal cancer outcome after surgery
Chelsea and Westminster Hospital0 个研究点目标入组 50 人开始时间: 2022年4月6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
- 50
研究概览
简要总结
2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37387798/ (added 03/07/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged 18 years and above, undergoing laparoscopic surgery with stage 2 or 3 colon cancer
- •2. Ability and willingness to consent
排除标准
- •1. Stage 1 and stage 4 colon or rectal cancer
- •2. Palliative surgery with no curative intent
- •3. Extensive comorbidities, i.e. American Society of Anesthesiologists (ASA) Score IV
- •4. Patients with known allergy to lidocaine
- •5. Patients who are pregnant or breastfeeding
- •6. Patients who are likely to have adverse effects from the accumulation of intravenous lidocaine:
- •6.1. Known liver disease with liver function outside the normal laboratory range
- •6.2. Epilepsy
- •6.3. Cardiac conduction abnormalities based on history and confirmed by electrocardiogram
研究者
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