NCT01652326已完成不适用
Clinical Quality Improvement of Benzodiazepine-Resistant Alcohol Withdrawal Syndrome
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 792
- 试验地点
- 1
- 主要终点
- Identify those risk factors predictive of benzodiazepine-resistant alcohol withdrawal syndrome
研究概览
简要总结
The overarching goal of this project is to improve the clinical quality of patients with Benzodiazepine-resistant alcohol withdrawal syndrome.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •a requirement of either 200 mg of diazepam (or diazepam equivalents) in 4 hrs;
- •> 40mg of diazepam (or diazepam equivalents) in 1 hr; or
- •an individual dose of 40 mg or greater of intravenous diazepam for control of agitation
排除标准
- •if < 18 years of age or had evidence of use of other illicit substances as determined by urine toxicology screen
研究组 & 干预措施
Benzodiazepine-resistant
those patients with either 1) a requirement of either 200 mg of diazepam (or diazepam equivalents) in 4 hrs; 2) >40mg of diazepam (or diazepam equivalents) in 1 hr; or 3) an individual dose of 40 mg or greater of intravenous diazepam for control of agitation
干预措施: Diazepam (Drug)
结局指标
主要结局
Identify those risk factors predictive of benzodiazepine-resistant alcohol withdrawal syndrome
时间窗: up to 38 months
次要结局
- Drug utilization of phenobarbital, propofol, dexmedetomidine, and ketamine in benzodiazepine-resistant alcohol withdrawal syndrome(Up to 38 months)
- Effectiveness of phenobarbital, propofol, dexmedetomidine, and ketamine in benzodiazepine-resistant alcohol withdrawal(Up to 38 months)
- Tolerability of phenobarbital, propofol, dexmedetomidine, and ketamine in benzodiazepine-resistant alcohol withdrawal(Up to 38 months)
研究者
研究点 (1)
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