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临床试验/CTRI/2026/03/105750
CTRI/2026/03/105750尚未招募4 期

Analgesic outcomes of Bupivacaine alone versus Bupivacaine with Dexmedetomidine in Bilateral Superficial cervical plexus block in Thyroid surgeries

Vinayaka Missions Kirupananda Variyar medical college and hospital Salem1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年4月1日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
40
试验地点
1

研究概览

简要总结

This prospective randomized comparative study aims to evaluate the analgesic outcomes of bilateral superficial cervical plexus block using bupivacaine 0.5Percent alone versus bupivacaine 0.5Percent with dexmedetomidine in patients undergoing elective thyroid surgery under general anesthesia. After induction an ultrasound guided superficial cervical plexus block will be performed. Postoperative pain will be assessed using the visual analogue scale and the duration of analgesia Time to first rescue analgesic Total analgesic requirement Hemodynamic parameters and Adverse effects will be recorded. The study seeks to determine whether the addition of dexmedetomidine enhances the quality and duration of postoperative analgesia compared to bupivacaine alone.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

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.Adult patients age 18 to 65 years undergoing elective thyroidectomy 2.American society of Anaesthesiologists physical status I or II 3.Written informed consent provided.

排除标准

  • 1.Allergy to study drugs 2.Coagulopathy or bleeding disorders 3.Chronic opioid use or substance abuse 4.Severe hepatic renal or cardiovascular disease Pregnancy or lactation.

研究者

发起方
Vinayaka Missions Kirupananda Variyar medical college and hospital Salem
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Senthil M

Vinayaka missions kirupananda variyar medical college and hospital

研究点 (1)

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