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临床试验/CTRI/2026/01/100318
CTRI/2026/01/100318尚未招募3 期

Comparison of Ultrasound-guided superficial cervical plexus block, greater auricular nerve block and local infiltration for postoperative analgesia in tympanomastoid surgery: A Randomized Controlled Trial

未提供1 个研究点 分布在 1 个国家目标入组 99 人开始时间: 2026年1月23日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
99
试验地点
1

研究概览

简要总结

This study aims to evaluate and compare the effectiveness of three different analgesic techniques used for pain control after tympanomastoid surgery. Postoperative pain after ear surgeries is often significant, and although opioids are commonly used, they are associated with adverse effects. Regional anesthesia techniques, particularly when performed using ultrasound guidance, can improve targeted pain relief and reduce the need for systemic analgesics. In this study, 99 patients aged 18 to 60 years undergoing tympanomastoid surgery will be randomly divided into three groups: one group will receive an ultrasound-guided superficial cervical plexus block, the second group will receive an ultrasound-guided greater auricular nerve block, and the third group will receive local anesthetic infiltration at the surgical site. Pain will be assessed at multiple intervals postoperatively using the Numerical Rating Scale, along with total analgesic consumption, incidence of postoperative nausea and vomiting, and patient satisfaction measured using a Likert scale. The study follows a randomized controlled design, with standard anesthetic management for all participants and clearly defined rescue analgesic protocols. Statistical analysis will include ANOVA for comparison of mean pain scores and Chi-square test for categorical outcomes. By directly comparing these commonly used analgesic methods, the study seeks to determine which approach provides the best postoperative pain control with minimal side effects, thereby improving recovery and overall patient comfort following tympanomastoid surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1 Patients aged 18 to 60 years 2 Patients undergoing tympanomastoid surgery 3 Patients under ASA I and ASA II physical status classification.

排除标准

  • 1 Refusal by patient for participation 2 Patients with previous history of migraine 3 Patients with previous history of head and neck surgeries 4 Patients with documented drug allergy to bupivacaine 5 If the duration of surgery is more than 4 hours.

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Usha Shukla

Uttar Pradesh University of Medical Sciences, Saifai, Etawah

研究点 (1)

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