ACTRN12605000231640终止3 期
A clinical trial of dexmedetomidine or remifentanil sedation for awake fibreoptic intubation
Dr Sarah Harper0 个研究点目标入组 20 人开始时间: 2005年8月26日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 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 ot stated（—）
- 性别
- All
入选标准
- •Awake fibreoptic intubation, no contraindication to remifentanil or dexmedetomidine.
排除标准
- •Chronic alpha-2 agonist or opioid therapy, allergy or previous adverse reaction to study drugs, uncontrolled hypertension, heart <50, 2nd or 3rd degree heart block, severe ventricular, renal, hepatic or respiratory dysfuction, pregnancy or lactation.
研究者
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