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临床试验/CTRI/2025/02/081174
CTRI/2025/02/081174
尚未招募
不适用

Comparison of ropivacaine with and without dexmedetomidine in infraclavicular brachial plexus block for postoperative analgesia in forearm surgeries

D Sanitha kumari1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年3月7日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
D Sanitha kumari
入组人数
40
试验地点
1
主要终点
1. Time for rescue analgesia

概览

简要总结

Summary:

This prospective, comparative study evaluates the efficacy of ropivacaine with and without dexmedetomidine for infraclavivular brachial plexus block in forearm surgeries, focusing on post-operative analgesia

Methodology:The patients are randomised into two groups (Group A and Group B) of 20 patients each using computer generated random number method. Group A patients will receive Plain 0.75% Ropivacaine and Group B patients will receive 0.75% Ropivacaine with 1μg/kg Dexmedetomidine

The following parameters will be recorded post-operatively at fixed time intervals:

-vas score

-Ramsay sedation score

-time for rescue analgesia

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

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

入选标准

  • 未提供

排除标准

  • Patient not giving consent Local skin infections Significant cardiac disease and patients on beta blockers.
  • Suspected coagulopathy or bleeding diathesis Allergy to local anesthetics and study drug.
  • Psychiatric Illness Chronic preoperative opioid consumption Procedure posted for other than supine position.

结局指标

主要结局

1. Time for rescue analgesia

时间窗: Measured post-operatively at regular intervals 0,4,8,12,16,20,24hours

次要结局

  • 1. Visual analog scale (VAS) score(2. Ramsay sedation score)

研究者

发起方
D Sanitha kumari
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

D Sanitha kumari

Dr. D.Y.Patil hospital and research center

研究点 (1)

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