NCT02180737已完成4 期
Evaluation of Role of Dexmedetomidine as a Sole Agent in Sedation of Cancer Patients Undergoing Radiological Interventional Procedures
National Cancer Institute, Egypt1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- verbal analogue scale
研究概览
简要总结
Evaluation of the role of dexmedetomidine as a sole agent in sedating patients undergoing interventional radiological procedures and measuring its different outcome variables.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age from 18-65 years old
- •ASA physical status of I-II
- •Expected procedure lasting at least 30 minutes
排除标准
- •Unstable cardiac status (life-threatening arrhythmias, abnormal cardiac anatomy, significant cardiac dysfunction and third-degree heart block.
- •An alpha2-agonist or antagonist within 14 days before the scheduled procedure.
- •patients received an IV opioid within 1 h, or an oral or IM opioid within 4 h of the start of study drug administration.
- •Patients who are allergic to Dexmedetomidine or alpha 2-agonists.
研究组 & 干预措施
Dexmeditomedine
Experimental
Dexmedetomidine will be initiated at 0.6 mcg/kg/hr and titrated to achieve desired clinical effect with doses ranging from 0.2 to 1 mcg/kg/hr.
干预措施: Dexmeditomedine (Drug)
结局指标
主要结局
verbal analogue scale
时间窗: 1 hour
assessment of pain using VAS score
Degree of sedation
时间窗: 1 hour
It will be measured and recorded by using the Ramsay sedation score.
次要结局
- patient satisfaction(24 hours)
研究者
Ghada M N Bashandy
Dr
National Cancer Institute, Egypt
研究点 (1)
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