TCTR20200325003Enrolling By Invitation1 期
A comparison of different dose intravenous lidocaine for prevent cough and sore throat after awakening from general anesthesia, a double blind randomized control trial
适应症
试验速览
- 阶段
- 1 期
- 状态
- Enrolling By Invitation
- 入组人数
- 184
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
- •â€¢ agree to receive treatment according to the research plan
- •â€¢ undergoing surgery By choosing the method of anesthesia and endotracheal tube
- •â€¢ Age 18-65 years
- •â€¢ ASA I-II (patients who do not have any underlying disease or have underlying disease that can control the symptoms and do not have severe complications)
- •â€¢ able to read, write and understand Thai
排除标准
- •â€¢ Refusing to participate in research
- •â€¢ have a history of hypersensitivity to lidocaine or other local anesthetics
- •â€¢ Patients with abnormal liver and kidney function
- •â€¢ Patients with congestive heart failure, recent myocardial infarction and cardiac arrhythmia such as AV block, atria fibrillation, Ventricular tachycardia
- •â€¢ Problems with communication using language (language barrier)
- •â€¢ Patients with a history of asthma or emphysema
- •â€¢ Patients with a history of upper respiratory infections within 2 weeks.
- •â€¢ Patients with high blood pressure and receiving ACEI
- •â€¢ Patients who are pregnant Or is breast-feeding
- •â€¢ The patient undergoes emergency surgery.
- •â€¢ • Patients with adverse effects from coughing, such as patients with increased intracranial pressure and rupture globe
- •â€¢ ASA classification 3 and above
研究者
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