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临床试验/ACTRN12623001171606
ACTRN12623001171606尚未招募3 期

Dexmedetomidine in Cardiac surgical intraoperative drug evaluation (DECIDE): a triple-blind, placebo-controlled, randomised trial evaluating whether dexmedetomidine improves: cognition, days alive and coma free in patients aged 65 years or older.

niversity of Sydney0 个研究点目标入组 1,100 人开始时间: 2023年11月13日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
1,100

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
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
65 Years 至 o limit(—)
性别
All

入选标准

  • 1.Adults undergoing cardiac surgery with cardiopulmonary bypass
  • 2.Age 65 years and older
  • 3.Sufficient English language to complete the cognitive testing in the opinion of the research team
  • 4.Willing and able to comply with all study requirements, including treatment, timing, and assessments.

排除标准

  • 1.Dementia (pre-existing confirmed clinical diagnosis)
  • 2.Known allergy to Dexmedetomidine (DEX)
  • 3.Second or third-degree heart block
  • 4.Heart rate less than 55 unless on concomitant beta blockade
  • 5.Renal dialysis within 30 days of surgery
  • 6.Life expectancy of less than 30 days regardless of surgery
  • 7.Preoperative mechanical support other than intra-aortic balloon pump
  • 8.Salvage surgery requiring cardiopulmonary resuscitation
  • 9.Child-Pugh class C liver Cirrhosis
  • 10.Serious medical or psychiatric conditions that might limit the ability of the patient to comply with the study procedures.
  • 11.Hearing loss, or medical or psychiatric condition that could preclude the ability of the patient to comply with study procedures.
  • 12.Prior enrolment in DECIDE trial in prior 12 months.

研究者

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