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临床试验/NCT06952309
NCT06952309尚未招募不适用

Effect of Intravenous Lidocaine Combined With Intratracheal Dexmedetomidine on Postoperative Throat Pain in Patients Undergoing Thyroid Cancer Surgery

Anqing Municipal Hospital0 个研究点目标入组 144 人开始时间: 2025年4月25日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
144
主要终点
The incidence and severity of postoperative sore throat

研究概览

简要总结

Objective: The present study was to investigate the effect of intravenous lidocaine combined with intratracheal dexmedetomidine on postoperative sore throat in patients undergoing thyroid cancer surgery.

Methods: Investigators enrolled 144 patients with American Society of Anesthesiologists (ASA) physical status I and II, aged 18-65 years, and scheduled for elective undergoing thyroid cancer surgery with general anesthesia. The participants were randomly assigned into four groups(n=36 each group): Group L received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia. Group D received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL). Group LD received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL). Group C received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia.The incidence and severity of postoperative sore throat were recorded in four groups at 1 h, 2 h, 6 h, 24 h and 48 h after operation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Thyroid cancer surgery with ASA grades I-II
  • Aged 18-65 years
  • The patient's communication is normal and they have a certain learning ability

排除标准

  • Severe respiratory and circulatory system diseases
  • There was bradycardia (HR < 60 beats/minute) or atrioventricular block before the operation
  • Nervous system disease
  • Mental and psychological disorders
  • Abnormal liver and kidney functions
  • Pregnant and lactating women

研究组 & 干预措施

Intravenous lidocaine

Experimental

Group L received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

干预措施: Intravenous lidocaine (Drug)

Intracheal dexmedetomidine

Experimental

Group D received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

干预措施: Intracheal dexmedetomidine (Drug)

Intravenous lidocaine combined with intracheal dexmedetomidine

Experimental

Group LD received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

干预措施: Intravenous lidocaine combined with intracheal dexmedetomidine (Drug)

Saline

Experimental

Group C received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

干预措施: Saline (NaCl 0,9 %) (placebo) (Drug)

结局指标

主要结局

The incidence and severity of postoperative sore throat

时间窗: at 1 hour, 2 hour, 6 hour, 24 hour and 48 hour after operation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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