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临床试验/NCT06963112
NCT06963112已完成1 期

Impact of Intraoperative Midazolam on Delirium Outcome of Elderly Patients (I-IMODE): a Multicentre Randomised Controlled Trial

Chinese PLA General Hospital5 个研究点 分布在 1 个国家目标入组 612 人开始时间: 2025年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
612
试验地点
5
主要终点
Incidence of postoeprative delirium

研究概览

简要总结

This study was a multicenter, randomized, double-blind, placebo-controlled trial to treat elderly surgical patients with low-dose midazolam or placebo for anesthesia induction. The incidence of postoperative 7-day delirium was assessed and compared between two groups, to provide valuable reference for clinical practitioners in the use of midazolam in elderly surgical patients.

详细描述

This study is a multicenter, randomized, double-blind, placebo-controlled trial. A total elderly patients who underwent elective non cardiac surgery were included in the plan and randomly divided into an intervention group and a control group. The intervention group patients were given 2mg midazolam injection (Jiangsu Enhua Pharmaceutical Co., Ltd.) during anesthesia induction; The control group patients were given equal volume physiological saline. Follow up assessment of postoperative delirium and anxiety will be conducted 1-7 days after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
65 Years 至 85 Years(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •65 ≤ Age ≤ 85 years old;
  • •Elective surgery under general anesthesia, with an estimated surgery time of ≥ 2 hours;
  • •Non cardiac surgery, non neurosurgical surgery;
  • •ASA grades I-III;
  • •Agree to participate and sign the informed consent form;

排除标准

  • •Preoperative history of comorbidities such as depression and schizophrenia;
  • •History of neurological disorders, moderate stroke;
  • •Long term use of benzodiazepines before surgery;
  • •BMI≤18.5/BMI≥30 kg/m2
  • •There is cognitive impairment, which is determined based on Mini Mental State Examination (MMSE) scores below the standard threshold;
  • •There are communication barriers, such as severe dementia, language barriers, and severe hearing or visual impairments;
  • •There are any contraindications for the use of midazolam (contraindications for patients with severe respiratory dysfunction, patients with severe liver and kidney damage, patients with sleep apnea syndrome, and patients known to be allergic to benzodiazepines);
  • •Preoperative severe liver and kidney dysfunction;
  • •Patients expected to enter the ICU after surgery;

研究组 & 干预措施

Saline group

Placebo Comparator

The control group patients were given 2 mL physiological saline during anesthesia induction.

干预措施: Saline (Drug)

Midazolam group

Experimental

The intervention group patients were given 2mg midazolam injection (Jiangsu Enhua Pharmaceutical Co., Ltd.) during anesthesia induction

干预措施: Midazolam (Drug)

结局指标

主要结局

Incidence of postoeprative delirium

时间窗: Postoperaitve Day 1-7

Confusion Assessment Method (CAM) to assess the incidence of postoperative delirium, including four features: acute change or fluctuation course of mental status; inattention; altered level of consciousness; disorganized thinking

Incidence of postoperative anxiety

时间窗: Postoperaitve Day 1-7

Generalized Anxiety disorder-7 (GAD-7) scale to assess the incidence of postoperative anxiety, with range from 0 to 21 scores, higher scores indicating more anxious.

次要结局

  • Intraoperative awareness of the occurrence(Surgery End)
  • Incidence of delayed extubation(Surgery End)
  • 1-Year mortlity(Postoperative 1 year)
  • Onset time of delirium episodes(Postoperative Day 1-7)
  • Frequency of delirium episodes(Postoperative Day 1-7)
  • Subtype of delirium episodes(Postoperative Day 1-7)
  • Anxiety severity(Postoperative Day 1-7)
  • Resting and movement pain scores(Postoperative Day 1-3)
  • Incidence of postoeprative nausea and vomiting(Postoperative 1-7)
  • Incidence of non delirium complications and all-cause mortality(Postoperative Day 1-30)
  • Length of hospital stay(Postoperative Day 1-30)

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hao Li

Professor

Chinese PLA General Hospital

研究点 (5)

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