跳至主要内容
临床试验/CTRI/2024/12/078757
CTRI/2024/12/078757尚未招募Phase 3 4

The effect of intravenous dexmedetomidine added to dexamethasone in patients undergoing proximal humeral fracture fixation under interscalene block: A double blind randomized placebo controlled trial.

Maharana Bhupal Government Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年1月11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
120
试验地点
1
主要终点
duration of post-operative analgesia(the time from block to rescue analgesic dose)

研究概览

简要总结

My thesis topic is -The effect of intravenous dexmedetomidine added to dexamethasone in patients undergoing proximal humeral fixation under interscalene block:A double blind randomized placebo controlled trial. It aims to explore the beneficial effects of addition of newer alpha2 agonist to routinely/ conventionally used drugs for regional blocks of upper limb.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

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

入选标准

  • consenting ASA physical status 1-3 patients scheduled to undergo unilateral ORIF proximal humeral fracture presenting at our hospital will be included in the study.

排除标准

  • Allergic to study drugs cogulopathy infection at the site of block chronic pain disorder patient refusal H/O cardiac,renal or hepatic disease preexisting neurological deficits of the involved arm neuropathy affecting the brachial plexus contraindications to peripheraal nerve block contralateral paresis of the phrenic or recurrent laryngeal nerves.

结局指标

主要结局

duration of post-operative analgesia(the time from block to rescue analgesic dose)

时间窗: upto 24 hrs postoperatively

次要结局

  • onset time of block,and 24 hour consumption of rescue analgesic(upto 24 hrs postoperatively)

研究者

发起方
Maharana Bhupal Government Hospital
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Vikram Bedi

RNT MEDICAL COLLEGE

研究点 (1)

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