ACTRN12614001215617撤回4 期
A double-blinded randomised clinical trial comparing the time of onset, duration and clinical effects of subcutaneous vs intravenous rocuronium in adult surgical patients
Fremantle Hospital0 个研究点目标入组 20 人开始时间: 2014年11月19日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 撤回
- 发起方
- 入组人数
- 20
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 64 Years（—）
- 性别
- All
入选标准
- •Elective or semi-elective surgery (surgery not required within 24 hours of being booked)
- •Expected duration of anaesthesia >6 hours
- •Planned admission to the intensive care unit after surgery
排除标准
- •Emergency surgery (surgery within 24 hours of procedure being booked)
- •Patients unable to give informed consent
- •Severe renal impairment (eGFR <30ml/min)
- •Significant hepatic impairment (known history of cirrhosis or liver dysfunction)
- •History of neuromuscular disease (e.g. poliomyelitis, myasthenia gravis, eaton-lambert syndrome)
- •Patients taking long term medications: lithium, phenytoin, carbamazepine
- •Administration of other muscle relaxant in previous 24 hours (suxamethonium or other non-depolarising muscle relaxant)
- •Pregnant or breastfeeding women
- •Patients requiring muscle relaxation to facilitate surgery
- •Patients having surgery where muscle relaxation is contraindicated
- •Significant possibility of anaesthetic ending prior to 6 hours (for instance – intra-abdominal surgery that may be abandoned due to disease progression that can only be decided after starting operation)
研究者
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