跳至主要内容
临床试验/TCTR20230222006
TCTR20230222006招募中4 期

Comparative Efficacy of Propofol Lidocaine Mixture alone with Fentanyl Pretreatment and Ondansetron Pretreatment for Propofol Lidocaine Mixture to Reduce Propofol induced Pain On Injection: A Double-Blinded Randomized Controlled Trial

eurological Institute of Thailand0 个研究点目标入组 111 人开始时间: 2023年2月22日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
111

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
18 Years 至 65 Years(—)
性别
All

入选标准

  • 1. Age 18 - 65 years
  • 2. Undergoing general anesthesia
  • 3. Elective surgery
  • 4. ASA physical status I or II

排除标准

  • 1. History of chronic pain
  • 2. The patient has a history of allergy to propofol, eggs, lidocaine, fentanyl, or ondansetron.
  • 3. Patients with liver disease
  • 4. Patient has communication problems
  • 5. The patient received anxiolytics or painkillers on the morning of the surgery.
  • 6. Body mass index
  • greater than or equal to 30 kilograms per square meter
  • 7. Rapid sequence intubation

研究者

发起方
eurological Institute of Thailand

相似试验