跳至主要内容
临床试验/CTRI/2017/11/010327
CTRI/2017/11/010327招募中不适用

Comparison of plain Ropivacaine versus Ropivacaine with different concentration of Dexmedetomidine in ultrasound guided supraclavicular block for Orthopedic forearm surgery-A prospective , randomised , comparative clinical study

Parul sevashram hospital1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2017年8月16日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
75
试验地点
1
主要终点
1. Duration of analgesia

研究概览

简要总结

Supraclavicular block of brachial plexus is commonly used block for Orthopedic forearm surgery. Ropivacaine is local anaesthetic agent that block peripheral afferents acting on voltage gated sodium channel. It provide good operative condition but have shorter duration of postoperative analgesia and good cardiovascular safety. Hence various adjuvants were added to local anaesthetic in brachial plexus block to achieve quick, dense and prolonged block. Dexmedetomedine, an alpha2 agonist is an adjuvant to local anaesthetic in regional anaesthesia to enhance quality and duration of analgesia. Dose range of 0.5 - 2microgm/kg has been used in various studies. The aim of study is to enhance safety and efficacy of plain Ropivacaine with different concentrations of dexmedetomedine.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

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

入选标准

  • 1.ASA grade 1 and 2 2.Both elective and emergengy surgeries.
  • 3.Upper limb surgeries-elbow,forearm and hand 4.Patient able to give informed and written consent.

排除标准

  • 1.Allergy or hypersensitivity to local anaesthtic agent
  • Patient with bleeding disorder or on anticoagulant therapy
  • Pregnant patient
  • Patient with major cardiovascular,respiratory ,renal,and liver disease
  • Patient taking opiod medicine.

结局指标

主要结局

1. Duration of analgesia

时间窗: 1. From end of surgery to pain on VAS OF 4 or more.. | 2. From onset of block to start of recovery

2. Duration of sensory and motor block

时间窗: 1. From end of surgery to pain on VAS OF 4 or more.. | 2. From onset of block to start of recovery

次要结局

  • Adverse effects, sedation score, rescue analgesic(Every 2 hourly upto 24 hrs)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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