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临床试验/NCT05280236
NCT05280236已完成不适用

Comparison of Quality of Recovery Between Remimazolam and Propofol Anesthesia in Patients Undergoing Arthroscopic Meniscectomy

Yonsei University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2022年3月14日最近更新:
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
80
试验地点
1
主要终点
Quality of Recovery (QoR)-40 questionnaire

研究概览

简要总结

This study aims to compare quality of recovery after surgery and anesthesia between patients undergoing arthroscopic meniscectomy under general anesthesia with either propofol or remimazolam based total intravenous anesthesia. This study is a randomized trial with a 50% probability of being assigned to either group. Randomization will be done by an anesthesiologist not involved in anesthesia or postoperative outcome assessment. Patients and the investigator in charge of postoperative outcomes assessment will be blinded to group allocation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients 19 or older, ASA class I~III,
  • scheduled for arthroscopic meniscectomy under general anesthesia and eligible for LMA use.

排除标准

  • Patient refusal,
  • patients unable to read consent form, active URI or uncontrolled asthma,
  • pneumonia,
  • history of allergies to propofol or benzodiazepines,
  • decreased liver or kidney function, heart failure of ejection fraction<55%,
  • pregnant or breastfeeding patients,
  • history of substance abuse/addiction

研究组 & 干预措施

Propofol

Active Comparator

Patients receiving general anesthesia with propofol-based total intravenous anesthesia

干预措施: Propofol TIVA (Drug)

Remimazolam

Experimental

Patients receiving general anesthesia with remimazolam-based total intravenous anesthesia

干预措施: Remimazolam TIVA (Drug)

结局指标

主要结局

Quality of Recovery (QoR)-40 questionnaire

时间窗: Postoperative 24 hours

Quality of recovery assessed with the QoR-40 questionnaire, which is a widely-used, self-rated, self-completed questionnaire for postoperative patients.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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