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临床试验/NCT06553495
NCT06553495进行中(未招募)不适用

A Comparative Analysis of Intertransverse Nerve Block and Paravertebral Nerve Block in Endoscopic Hepatectomy

Jie Chen1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
80
试验地点
1
主要终点
The number of effective compressions of the analgesic pump within 24 hours after surgery

研究概览

简要总结

This study aims to compare the analgesic effect of intertransverse nerve block and paravertebral nerve block after endoscopic hepatectomy, evaluate its effectiveness and safety, and provide new ideas and clinical basis for postoperative pain management of liver surgery.

详细描述

This study was a prospective, double-blind, randomized controlled trial. Patients who were eligible for laparoscopic partial liver resection in our center were included, with intertransverse nerve block as the experimental group and paravertebral nerve block as the control group. Through the analysis of postoperative pain score 30min to 24h, the number of effective analgesic pump compressions within 24h, the amount of analgesic drugs used, complications and other data, To evaluate the efficacy and safety of intertransverse nerve block in patients undergoing laparoscopic partial liver resection.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 1.18-80 years old adult, BMI<27.9kg/m2
  • American Society of Anesthesiologists ASA Grade I-III
  • Patients with laparoscopic partial liver resection such as liver tumors
  • Willing to participate in this study and sign the informed consent form

排除标准

  • The patient or family member refuses to sign the informed consent form
  • Blood coagulation dysfunction, local infection
  • Those who have communication, communication disorders or mental abnormalities
  • Patients with severe heart, pulmonary and renal insufficiency or patients with central system diseases
  • For any reason, it cannot be matched with the study or the researcher believes that it is not appropriate to be included in this experiment.

结局指标

主要结局

The number of effective compressions of the analgesic pump within 24 hours after surgery

时间窗: Within 24 hours after the operation

次要结局

未报告次要终点

研究者

发起方
Jie Chen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jie Chen

临床教授

The Second Affiliated Hospital of Chongqing Medical University

研究点 (1)

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