跳至主要内容
临床试验/JPRN-UMIN000009665
JPRN-UMIN000009665已完成4 期

Effect of dexmedetomidine on death and duration of mechanical ventilation in sepsis patients under lighter sedation randomized controlled trial - Dexmedetomidine for sepsis in ICU Randomized Evaluation trial(DESIRE trial)

Research Organization for Sedation at Emergency and critical care0 个研究点目标入组 200 人开始时间: 2013年1月10日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
200

研究概览

简要总结

Question Does a sedation strategy with dexmedetomidine compared with no dexmedetomidine improve ventilator-free days and mortality among patients with sepsis requiring ventilation? Findings In this randomized clinical trial that included 201 adults, treatment with dexmedetomidine compared with treatment without dexmedetomidine did not significantly improve ventilator-free days (20 days vs 18 days) or 28-day mortality (23% vs 31%; hazard ratio, 0.69). Meaning Treatment with dexmedetomidine in patients with sepsis did not improve either ventilator-free days or 28-day mortality.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Severe chronic liver disease(Child B or C) Acute myocardial infarction, heart disease(New York Heart Association[NYHA] 4) Drug dependence, alcoholism Psychological illness, severe cognitive dysfunction Pregnant or lactating women Patients who have allergy for dexmedetomidine Attending physician's decision

研究者

发起方
Research Organization for Sedation at Emergency and critical care

相似试验