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临床试验/CTRI/2025/03/083676
CTRI/2025/03/083676尚未招募不适用

Postoperative Analgesic Efficacy of Ultrasound-Guided Erector Spinae Plane Block versus Local InfiltrationAnalgesia in Patients Undergoing Lumbar Spine Fixation under General Anaesthesia: A Randomised Double BlindTrial

Sir Ganga Ram Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年4月18日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
70
试验地点
1
主要终点
First rescue analgesia

研究概览

简要总结

This randomized, double-blind, parallel-group, single-center trial compares the efficacy of ultrasound-guided erector spinae plane (ESP) block to local infiltration analgesia (LIA) with 0.25% Levobupivacaine in patients undergoing lumbar spine fixation surgery under general anesthesia. The primary outcome is the time to first rescue analgesia post-surgery. Secondary outcomes include hemodynamic parameters (mean arterial pressure and heart rate) at various intervals up to 24 hours post-surgery, postoperative pain scores using the Numerical Rating Scale (NRS), functional recovery (time to first ambulation and self-voiding), patient satisfaction for pain relief using a 5-point Likert scale, and postoperative nausea and vomiting (PONV) scores at 0.5, 1, 2, 6, 12, and 24 hours post-surgery.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1 or 2 level spine fixation surgeries Body mass index (BMI).
  • 18-30 kg/m2 American Society of Anaesthesiology (ASA) Grade.

排除标准

  • Refusal of consent to participate in study More than 2 level of spine fixation surgery Coagulation disorders(INR more than 1.5) History of hypersensitivity to local or systemic anaesthetic agents Block Failure.

结局指标

主要结局

First rescue analgesia

时间窗: in postoperative period within 24 hours

次要结局

  • Hemodynamic parameters, Postoperative pain scores, Functional recovery,(Patient satisfaction & PONV)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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