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临床试验/NCT06574945
NCT06574945已完成4 期

Efficacy and Safety of Propofol in Combination With Different Esketamine Doses for Anesthesia During Loop Electrosurgical Excision Procedure

Qian Wu1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年1月7日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
90
试验地点
1
主要终点
Respiratory Rate

研究概览

简要总结

The goal of this prospective, randomized controlled study study is to investigate the efficacy and safety of propofol combined with different doses of esketamine (ESK) for anesthesia during loop electrosurgical excision procedure (LEEP).Ninety female patients undergoing LEEP were randomly allocated to three groups.It aims to answer :1.The effect of esketamine combined with propofol in respiration, circulation, etc,during LEEP. 2.The appropriate dosage of esketamine when combined with propofol in LEEP anesthesia.

详细描述

To investigate the efficacy and safety of propofol combined with different doses of esketamine (ESK) for anesthesia during loop electrosurgical excision procedure (LEEP). Ninety female patients undergoing LEEP were randomly allocated to three groups: group P (2 mg/kg propofol + saline), group propofol + esketamine(PK)1 (1.5 mg/kg propofol + 0.5 mg/kg ESK), and group PK2 (1.5 mg/kg propofol + 0.25 mg/kg ESK). Parameters including mean arterial pressure (MAP), heart rate (HR), respiratory rate (RR), oxygen saturation (SPO2), and venous carbon dioxide (PvCO2) were recorded. Additionally, the need for supplemental propofol, jaw thrust maneuver or ventilation, postoperative awakening time, and adverse reactions were assessed.

研究设计

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

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Patients who refused to participate
  • History of hypertension, hyperthyroidism, or neurological or mental disorder
  • Currently taking or has taken opioids and non-steroidal anti-inflammatory drugs within 48 h before surgery
  • Participated in other drug clinical trials within 4 weeks
  • Allergy to esketamine or propofol
  • History of opioid or esketamine addiction

研究组 & 干预措施

group PK1

Experimental

Intravenous injection of 0.5 mg/kg esketamine followed by 1.5 mg/kg of propofol

干预措施: intravenous injection of propofol +esketamine (Drug)

group P

Placebo Comparator

Intravenous injection of an equivalent dose of normal saline followed by 2 mg/kg of propofol

干预措施: intravenous injection of propofol only (Drug)

group PK2

Experimental

Intravenous injection of 0.25 mg/kg esketamine followed by 1.5 mg/kg of propofol

干预措施: intravenous injection of propofol +esketamine (Drug)

结局指标

主要结局

Respiratory Rate

时间窗: Immediately upon entering the operating room , 1 and 5 minutes after injection of anesthetics

The respiratory rate (RR) was monitored from 3-lead ECG

Heart Rate

时间窗: Immediately upon entering the operating room , 1 and 5 minutes after injection of anesthetics

The heart rate (HR) was monitored using 3-lead ECG

Mean Arterial Pressure

时间窗: Immediately upon entering the operating room, 1 and 5 minutes after injection of anesthetics

The mean arterial pressure (MAP) was monitored using Noninvasive blood pressure monitor

Venous Carbon Dioxide

时间窗: Immediately upon entering the operating room and 5 minutes after injection of anesthetics

The venous carbon dioxide (PvCO2) was monitored using blood-gas analyzer

次要结局

  • number of jaw thrust maneuver or face mask ventilation(On the day of surgery, from the instant the anesthesia induction is completed to the instant completion of surgery,up to 10 minutes)
  • incidences of postoperative vertigo, nausea, agitation and delirium(On the day of surgery,from the moment the patient wakes up (when MOAA score >4) to the moment the patient leaving the recovery room,up to 30minutes)
  • number of additional propofol usage(On the day of surgery, from the instant the anesthesia induction is completed to the instant completion of surgery,up to 10 minutes)
  • postoperative awakening time(On the day of surgery, from the instant completion of surgery to the moment the patient wakes up (when MOAA score >4),up to 10 minutes)

研究者

发起方
Qian Wu
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Qian Wu

Principal Investigator

First Affiliated Hospital of Chongqing Medical University

研究点 (1)

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