跳至主要内容
临床试验/CTRI/2021/11/038117
CTRI/2021/11/038117尚未招募4 期

A COMPARATIVE STUDY BETWEEN DEXMEDETOMIDINE VERSUS DEXAMETHASONE AS ADJUVANT TO 0.5% ROPIVACAINE IN ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUS BLOCK

Dr Anukrishna K V1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2021年11月19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
62
试验地点
1
主要终点
To assess the onset of sensory blockade and motor blockade, duration of sensory and motor blockade, duration of analgesia

研究概览

简要总结

This is a comparative study between 2 drugs- dexmedetomidine and dexamethasone when added to another drug ropivacaine when used in ultrasound guided supraclavicular brachial plexus block. Monitoring will be done for onset and duration of sensory and motor blockade,  and will be monitored postoperatively for duration of analgesia. Changes in vitals also will be recorded.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Weight between 45 to 70Kgs, posted for elective and emergency surgeries below midarm, forearm and hand will be included.

排除标准

  • History of infection at site of block, history of coagulopathies, patients with known hypersensitivity to local anaesthetic or any study drug, patient with known hypersensitivity to local anaesthetic or any study drug, Patient with presence of 1st, 2nd or 3rd degree heart block, Pregnant women, Patient with pre-existing peripheral neuropathy.

结局指标

主要结局

To assess the onset of sensory blockade and motor blockade, duration of sensory and motor blockade, duration of analgesia

时间窗: 0,5, 10, 15, 20, 40, 60, 80, 100, 120, 140, 160 400, 640, 880, 1360, 1600 minutes

次要结局

  • To assess the total consumption of rescue analgesia in 24 hour postoperatively and to monitor hemodynamic stability(0,5, 10, 15, 20, 40, 60, 80, 100, 120, 140, 160 400, 640, 880, 1360, 1600 minutes)

研究者

发起方
Dr Anukrishna K V
申办方类型
Other [self]

研究点 (1)

Loading locations...

相似试验