跳至主要内容
临床试验/TCTR20191125001
TCTR20191125001已完成4 期

Comparison of the effects of intravenous propofol and intravenous propofol with low dose of ketamine on preventing post-extubation cough and laryngospasm in patient awakening from general anesthesia: a prospective randomized clinical trial.

Phramongkutklao Hospital0 个研究点目标入组 120 人开始时间: 2019年11月25日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
120

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 80 Years(—)
性别
All

入选标准

  • ASA physical status I and II, with airway assessment of Mallampati grade 1 and 2, between the age group of 18-60 years, scheduled for elective surgeries under general anesthesia.

排除标准

  • unwilling patients, history of allergy to any drug, history of bronchial asthma, chronic obstructive pulmonary disease, respiratory tract infection, impaired kidney or liver function, on angiotensin converting enzyme inhibitors, a history of hypersensitivity to local anesthetics, pregnancy and language barrier.

研究者

相似试验