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临床试验/NCT06165848
NCT06165848已完成不适用

Effects Of Different Anesthesia Applications On Mood, Depression, And Anxiety Levels In Burn Patients

T.C. Sağlık Bakanlığı Ankara Bilkent Şehir Hastanesi1 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2020年7月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
67
试验地点
1
主要终点
Montgomery-Asberg Depression Rating Scale (MADRS),

研究概览

简要总结

Adequate and effective pain management and prevention of depression are essential in burn patients. This study aims to investigate the effects of ketamine sedation in burn patients in terms of mood disorders, depression, anxiety, and suicidal tendency during intensive care follow-up in the postoperative period.

详细描述

Aim: Adequate and effective pain management and prevention of depression are essential in burn patients. This study aims to investigate the effects of ketamine sedation in burn patients in terms of mood disorders, depression, anxiety, and suicidal tendency during intensive care follow-up in the postoperative period.

Methods: The study was conducted with 67 patients between 18 and 65 years of age, who were ASA I-II class, had basic communication skills, no previous diagnosis of psychiatric illness, and no history of neuropsychiatric or cognitive disease or related treatment. After preoxygenation, anesthesia induction was performed with 2 mg/kg IV propofol and 1 mcg/kg IV fentanyl in the general anesthesia group. Anesthesia was continued with a mixture of 0.3-0.5 mcg/kg/min remifentanil, 2% sevoflurane, 50% air, 50% oxygen. In the sedation group, 1 mcg/kg IV fentanyl and 1 mg/kg IV ketamine were administered at induction; anesthesia was maintained by adding 30-50 mg IV propofol if necessary. The Montgomery-Asberg Depression Rating Scale (MADRS), the Hamilton Anxiety Rating Scale (HAM-A), and the Beck Scale for Suicide Ideation (BSSI) were administered preoperatively and on postoperative day one by the psychiatrist.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Who were ASA I-II class,
  • Had basic communication skills,
  • No previous diagnosis of psychiatric illness,
  • No history of neuropsychiatric or cognitive disease or related treatment.

排除标准

  • With a previous diagnosis of psychiatric illness,
  • Neuropsychiatric or cognitive illness,
  • Or a history of related treatment.

结局指标

主要结局

Montgomery-Asberg Depression Rating Scale (MADRS),

时间窗: 72 hours

In order to determine whether there is negative mood and depression; Montgomery-Asberg Depression Rating Scale (MADRS) was administered by the psychiatrist .

Hamilton Anxiety Rating Scale (HAM-A)

时间窗: 72 hours

For anxiety; Hamilton Anxiety Rating Scale (HAM-A) was administered by the psychiatrist .

Beck Suicidal Ideation Scale (BSSI)

时间窗: 72 hours

To determine whether there is suicidal ideation; Beck Suicidal Ideation Scale (BSSI) was administered by the psychiatrist .

次要结局

未报告次要终点

研究者

发起方
T.C. Sağlık Bakanlığı Ankara Bilkent Şehir Hastanesi
申办方类型
Other
责任方
Sponsor

研究点 (1)

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