跳至主要内容
临床试验/CTRI/2022/06/043470
CTRI/2022/06/043470尚未招募Phase 3 4

The analgesic effect of Nalbuphine as an adjuvant to 0.5% Ropivacaine in Ultrasound Guided Supraclavicular Brachial Plexus Nerve Blocks : a prospective interventional study at SMS Hospital, Jaipur during 2021-2023.

Department of Anaesthesia1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2022年6月24日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
入组人数
64
试验地点
1
主要终点
Duration of post-operative analgesia according to NRS scale.(time of first request of rescue analgesia).

研究概览

简要总结

In this double blinded randomized controlled interventional study, we will compare the analgesic effect of nalbuphine as an adjuvant to 0.5% ropivacaine in ultrasound guided supraclavicular brachial plexus nerve blocks  with the analgesic effect of 0.5% ropivacaine alone in ultrasound guided supraclavicular brachial plexus nerve blocks .

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 50.00 Year(s)(—)
性别
All

入选标准

  • 1.participant of fracture forearm surgeries under USG guided supraclavicular block.
  • ASA physical status class 1and 2 .
  • patients willing to participate.

排除标准

  • Patients with a history of allergy or hypersensitivity to either local anaesthetics or opioid group of drugs.
  • Any contra indication to peripheral nerve block.
  • 3.impaired ability to communicate.
  • 4.patients with raised intracranial tension.
  • 5.pregnancy.
  • 6.patient with coagulation disorder.
  • 7.local infection/swelling at the site of injection.

结局指标

主要结局

Duration of post-operative analgesia according to NRS scale.(time of first request of rescue analgesia).

时间窗: Every 30 minutes in first hour then every one hourly in next twelve hours.

次要结局

  • Proportion of cases with complications(Post operative period)
  • Side-effects(If any)
  • Mean duration of analgesia(In post-operative period)
  • Haemodynamic parameters(Intraoperative period)

研究者

申办方类型
Government medical college

研究点 (1)

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