跳至主要内容
临床试验/CTRI/2026/04/107988
CTRI/2026/04/107988尚未招募4 期

Comparison of efficacy of adding doses of Nalbuphine to Bupivacaine for brachial plexus block for upper limb Surgeries A Randomised Control trial

Heritage Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2026年4月21日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
72
试验地点
1

研究概览

简要总结

This a Double blinded Randomised control trial study compares efficacy of 5mg vs 10mg Nalbuphine(1 ml) with 0.375% bupivacaine (19 ml)  for Supraclavicular brachial plexus block in upper limb surgeries,Aim of study is to assess onset of action and duration of action of both groups of patients and duration of postop analgesia

研究设计

研究类型
Interventional
分配方式
Randomized
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

  • Eligible age group for study 18-65 years old of weight 50-90 kg.
  • Eligible gender for study Both Male and Female ASA physical status classification I-II Patients scheduled for elective upper limb surgery.

排除标准

  • Patients denying consent for study.
  • Diabetic neuropathy.
  • Known nerve injury in the upper limb posted for surgery.
  • Known contraindications to regional anaesthetic techniques as coagulopathy.
  • ASA physical status class III-IV.
  • Skin infection at site of anaesthesia.
  • Known hypersensitivity to the drugs used in studies.

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Subham jasiwal

Heritage institute of medical sciences

研究点 (1)

Loading locations...

相似试验