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临床试验/TCTR20190704003
TCTR20190704003尚未招募1 期

The Efficacy of risperidone oral solution for reducing the incidence of postoperative delirium in vascular patients: a randomized controlled trial

Faculty of Medicine Siriraj Hospital, Mahidol University0 个研究点目标入组 140 人开始时间: 2019年7月4日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
60 Years 至 0 N/A (No limit)(—)
性别
All

入选标准

  • 1. patients aged > 60 years
  • 2. undergoing elective vascular surgery
  • 3. operative time > 2 hours.

排除标准

  • 1. patients with cognitive impairment (a Thai Mental State Examination score < 24)
  • 2. evidence of alcohol abuse
  • 3. alcohol ingestion occurring in the 14-day period preceding the surgery
  • 4. preoperative delirium (shown by a positive result with the Confusion Assessment Method for the Intensive Care Unit, CAM-ICU)
  • 5. severely impaired renal function (demonstrated by a creatinine clearance < 30 mL/min/1.72 m2)
  • 6. hepatic impairment (a Child Pugh score ≥ 10)
  • 7. allergy to risperidone
  • 8. neuroleptic malignant syndrome

研究者

发起方
Faculty of Medicine Siriraj Hospital&#44; Mahidol University

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