跳至主要内容
临床试验/CTRI/2024/04/065598
CTRI/2024/04/065598尚未招募不适用

COMPARISON OF ANALGESIC EFFICACY OF LOCAL WOUND INFILTRATION WITH LEVOBUPIVACAINE PLUS DEXMEDETOMIDINE AND ROPIVACAINE PLUS DEXMEDETOMIDINE IN LOWER ABDOMINAL SURGERIES: A RANDOMISED CONTROLLED TRIAL

Dr G Vignesh1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年4月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
120
试验地点
1
主要终点
To Compare the efficacy of post operative analgesia of two drugs at 30mins,4hrs,8hrs,12hrs,20hrs,

研究概览

简要总结

To compare the better analgesic efficacy of infiltration of the two drugs with additives i.e., levobupivacaine with dexmedetomidine and ropivacaine with dexmedetomidine for postoperative pain relief in patients undergoing lower abdominal surgeries

Levobupivacaine with dexmedetomidine and ropivacaine with dexmedetomidine were the two drugs with adjuvants used for better post operative pain relief and reduce the frequency of rescue analgesia.

Purpose of this study to get better post operative pain relief and reduce the frequency of rescue analgesia and it is cost effective also.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator 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

  • Patients with ASA classification I & II Age of 18 to 60yrs Posted for elective lower abdominal surgeries Surgical duration of 1hr to 2hrs.

排除标准

  • Patient Refusal Allergic to local anaesthetics Failed Sub Arachnoid Block getting converted to GA Patchy Sub Arachnoid Block Obese Individual Lower Segment Caesarean Section.

结局指标

主要结局

To Compare the efficacy of post operative analgesia of two drugs at 30mins,4hrs,8hrs,12hrs,20hrs,

时间窗: To Compare the efficacy of post operative analgesia of two drugs at 30mins,4hrs,8hrs,12hrs,20hrs, | 24hrs and their analgesic duration

24hrs and their analgesic duration

时间窗: To Compare the efficacy of post operative analgesia of two drugs at 30mins,4hrs,8hrs,12hrs,20hrs, | 24hrs and their analgesic duration

次要结局

  • Frequency of rescue analgesia whenever VAS score more than or equal to 4 in first 24hrs(4hrs,8hrs,12hrs,20hrs,)

研究者

发起方
Dr G Vignesh
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr G Vignesh

Karpaga Vinayaga Institute Of Medical Sciences and Research Centre

研究点 (1)

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