跳至主要内容
临床试验/CTRI/2018/08/015353
CTRI/2018/08/015353尚未招募不适用

Comparative analgesic efficacy of pre-emptive oral clonidine and oral pregabalin in patients undergoing upper limb surgeries under supraclavicular block.A randomised,controlled prospective study.

Dr RPGMC Kangra at Tanda1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年8月26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
90
试验地点
1
主要终点
To study and compare block characteristics and rescue analgesic requirement with pre-emptive oral clonidine and oral pregabalin.

研究概览

简要总结

Study Title: Comparative analgesic efficacy of pre-emptive oral clonidine and oral pregabalin in patients undergoing upper limb surgeries under supraclavicular block: A randomized, controlled, prospective study.

Patients fulfilling the inclusion/exclusion criteria would be divided into three groups by block randomization and would receive clonidine 200mcg tablets, pregabalin 150mg tablets and placebo [colour matched B complex tablets] respectively. Patients will be assessed for a time duration of 24 hours for effect of pre-emptive oral clonidine and oral pregabalin on block characteristics (sensory motor onset and duration), post-operative rescue analgesic requirement, post-operative sedation and patient’s satisfaction.

研究设计

研究类型
Interventional
分配方式
Permuted block randomization, fixed
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.Scheduled for upper limb surgeries under supraclavicular block.
  • ASA Grade I-II.
  • BMI 18.5-29.9.

排除标准

  • Patient’s refusal for block
  • Patients with known drug allergy to study
  • Patients who have taken analgesics 48hrs before
  • Use of antiepileptics drugs
  • Hepatic and renal pathologies affecting drug clearence
  • History of long term usage of NSAIDs and opioid analgesics
  • Patient in whom the block effect will be partial and will require supplementary analgesic
  • Diabetes mellitus and other neuropathic disorders
  • Any contraindications for peripheral nerve blocks
  • Coagulopathy disorders
  • Psychiatric disorders
  • Addiction to any drug.

结局指标

主要结局

To study and compare block characteristics and rescue analgesic requirement with pre-emptive oral clonidine and oral pregabalin.

时间窗: 24hours

次要结局

  • To study and compare post-operative sedation and patient satisfaction.(24hours)

研究者

发起方
Dr RPGMC Kangra at Tanda
申办方类型
Government medical college

研究点 (1)

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