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临床试验/NCT05772832
NCT05772832已完成不适用

COMPARISON OF DEXMEDETOMIDINE AND REMIFENTANIL FOR POSTOPERATIVE PAIN IN TRANSPHENOIDAL Pituitary SURGERY

Kocaeli University1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2021年11月17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
104
试验地点
1
主要终点
postoperative pain scale

研究概览

简要总结

In patients with pituitary adenoma scheduled for endoscopic transsphenoidal pituitary surgery, it was aimed to compare the efficacy of postoperative pain relief of a selective α-2 agonist "Dexmedetomidine" and the rapid and short-acting opioid "Remifentanil" using the "Numerical Rating Scale" (NRS) administered alongside propofol in perioperative maintenance anesthesia. .

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

  • 18-65 years old
  • ASA-1 and ASA-2 patients

排除标准

  • Patients in need of postoperative intensive care

研究组 & 干预措施

GROUP USING REMIFENTANYL

THE GROUP USING PEROPERATIVE REMIFENTANYL AND PROPOFOL IN TRANSSPHENOIDAL Pituitary Surgery 0.01-0.2 μg /kg /min Remifentanyl and 3-12 mg/kg/h propofol

干预措施: Remifentanyl (Drug)

GROUP USING DEXMEDETOMIDINE

THE GROUP USING PEROPERATIVE DEXMEDETOMIDINE AND PROPOFOL IN TRANSSPHENOIDAL Pituitary Surgery 0.01-0.02 μg/kg/min (~0.5 μg/kg/h) continuous infusion of dexmedetomidine 1 mcg/kg 10 minutes after a loading dose and 3-12 mg/kg/h propofol

干预措施: Dexmedetomidine (Drug)

结局指标

主要结局

postoperative pain scale

时间窗: 24 hours after surgery (T4)

Comparison of postoperative Numerical Rating Scale(NRS) values of both study arms(min 0, max 10; 10 is unbearable pain )

次要结局

  • Comparison of postoperative nausea-vomiting rate(24 hours after surgery (T4))
  • need for analgesics(Additional analgesic drug requirements at 24 hours after surgery (T4))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

İpek İZGİN AVCI

principal investigator

Kocaeli University

研究点 (1)

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