跳至主要内容
临床试验/CTRI/2018/04/013254
CTRI/2018/04/013254招募中不适用

Comparison of fentanyl and dexmedetomidine as an adjuvant to bupivacaine in ultarsound guided supraclavicular brachial plexus block in upper limb surgeries: a randomized-double blind prospective study

Bhagat Phool Singh Government Medical College For Women1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2017年8月26日

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
64
试验地点
1
主要终点
1.Analgesic Efficacy in terms of Onset And Duration Of Motor And Sensory Blockade

研究概览

简要总结

In thisrandomized double blinded prospective study we intend to examine the effects ofdexmedetomidine v/s fentanyl as an adjuvant to bupivacaine on duration of themotor block, sensory block, and duration of analgesia and side effects in upperlimb surgeries along with their sedative effects.

64 ASA I-IIIpatients will be divided in two groups of 32 each after they fulfill theinclusion and exclusion criteria of the study. Each group will receivedifferent adjuvant drug for Ultrasound Guided Supraclavicular block and effectsof the same will be observed. And onset time and total duration of motor andsensory block in both groups will be calculated.and comparison of side effectsin both group will be done.

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 65.00 Year(s)(—)
性别
All

入选标准

  • American Society of Anesthesiologist’s Grades I to III
  • Patients of either sex
  • Aged 18-65 years.

排除标准

  • 1.Patients with known hypersensitivity to local anesthetic drugs 2.Bleeding disorders 3.Pre-existing neuropathy 4.Any hepatic, renal, neurological, psychiatric, or neuromuscular diseases 5.Minor/ pregnancy/ lactation/more than 65 years age will be excluded from the study.

结局指标

主要结局

1.Analgesic Efficacy in terms of Onset And Duration Of Motor And Sensory Blockade

时间窗: From The Time Of Drug Delivery To 24 Hours Of Postoperatively

次要结局

  • Intraoperative Vitals and Heart Rate , Blood Pressure , Sedation Till 24 Hours Postoperatively(From The Time Of Drug Delivery To 24 Hours Of Postoperatively)

研究者

发起方
Bhagat Phool Singh Government Medical College For Women
申办方类型
Government medical college

研究点 (1)

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