跳至主要内容
临床试验/CTRI/2025/10/096303
CTRI/2025/10/096303尚未招募Phase 3 4

Postoperative analgesic efficacy of 0.25% Ropivacaine with Dexmedetomidine versus Dexamethasone as adjuvants in Bilateral superficial cervical plexus block for Thyroidectomy surgery under general anesthesia-Randomized controlled trial

Dr Moopen’s Medical College, Wayanad1 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2025年11月1日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
86
试验地点
1
主要终点
To Understand which among the two adjuvants offers superior postoperative analgesia,fewer complications and better patient satisfaction

研究概览

简要总结

Thyroidectomy,a common elective surgery,often results in significant postoperative pain,which can impact recovery and patient comfort.The bilateral superficial cervical plexus block(BSCPB) is commonly used as an adjunct to general anesthesia to reduce postoperative pain in thyroid surgeries.To enhance the efficacy and duration of analgesia,adjuvants like dexmedetomidine and dexamethasone are often added to local anesthetics such as ropivacaine.

This randomized,single blinded,prospective,comparative study aims to evaluate and compare the analgesic efficacy of dexmedetomidine vs dexamethasoneas adjuvants to  ropivacaine-based BSCPB in patients undergoing elective thyroidectomy under general anesthesia.The study will be conducted at Dr Moopens Medical College,Wayanad,over a period of 1.5 years,involving86 ASA I&II patients aged 18-60 years,randomized into two equal groups.

The primary objective is to assess postopeartive pain using the Numerical Rating Scale(NRS) and determine the effectiveness of each adjuvant in prolonging analgesia and reducing the need for rescue analgesics.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant 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

  • Elective thyroidectomy surgery Belonging to ASA Class 1&2.

排除标准

  • Patients with altered cervical plexus anatomy Coagulation disorders Systemic infection and infection at injection site History of allergy to local anesthetic agents.

结局指标

主要结局

To Understand which among the two adjuvants offers superior postoperative analgesia,fewer complications and better patient satisfaction

时间窗: Time points used for Postoperative Analgesia comparison is zeroth hour( immediately after coming out of general anesthesia),2 hours ,6hours,12 hours and 24 hours

次要结局

  • To compare the total analgesic consumption within the twogroups(Within the first 24 hours after surgery)
  • To assess intraoperative hemodynamic stability in both groups(Throughout the surgey)
  • To compare the incidence of side effects/complications related to the block & adjuvants(Within the first 24 hours after the surgery)

研究者

发起方
Dr Moopen’s Medical College, Wayanad
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Drisya pv

Dr Moopen’s Medical College, Wayanad

研究点 (1)

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