To compare the effect of dexmeditomedine and fentanyl as an adjuvant to bupivacaine in peripheral nerve stimulator guided interscalene brachial plexus block in shoulder surgeries.

JNMC1 个研究点分布在 1 个国家目标入组 50 人开始时间: 2026年5月1日最近更新: 2026年4月2日

试验速览

阶段: 2 期
状态: 尚未招募
发起方
入组人数: 50
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

This study aims to compare the efficacy of dexmedetomidine and fentanyl as adjuvants to bupivacaine in peripheral nerve stimulator-guided interscalene brachial plexus block in patients undergoing elective shoulder surgeries.

A total of 50 patients will be randomly allocated into two groups to receive either dexmedetomidine or fentanyl along with bupivacaine. The study will evaluate onset and duration of sensory and motor block, duration of postoperative analgesia, hemodynamic parameters, and any adverse effects.

The objective is to determine which adjuvant provides better analgesia and block characteristics with minimal side effects.

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 50.00 Year(s)（—）
性别: All

入选标准

•ASA physical status 1 and 2 Patient undergoing elective shoulder surgeries Duration of surgery 120-180 minutes.

排除标准

•Patient refusal Allergy to local anaesthetic and opioids Local infection at the site of block Pregnant women Severe cardiopulmonary disease Patient with neurological deficit in operating arm.

研究者

发起方

JNMC

申办方类型

Private medical college

责任方

Principal Investigator

主要研究者

Avani Pareek

Dutta Meghe Institute of Medical and Research

研究点 (1)

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