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临床试验/CTRI/2021/01/030277
CTRI/2021/01/030277招募中不适用

A Comparative Efficacy of Addition of Fentanyl v/s Neostigmine toIsobaric 0.25% Bupivacaine in USG Guided Supraclavicular BrachialPlexus Block in Upper Limb Surgeries

NOT APPLICABLE1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年1月17日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
DURATION OF ANALGESIA

研究概览

简要总结

This study is  designed to  

  1. To find out the comparative efficacy of bupivacaine with fentanyl vs bupivacaine with neostigmine for onset, duration of sensory and motor block with duration of analgesia.
  2. To observe side effects of drugs among the different groups.

Fentanyl  has been used for regional nerve plexus blocks to improve the block duration and quality. The peripheral administration of opioids provides effective and long lasting analgesia without central side effects.Studies have shown better block duration and success rate of brachial plexus block on addition of fentanyl. Whereas neostigmine decreases the breakdown of acetylcholine by its inhibitory action on acetylcholinesterase, preclinical data suggests peripheral anti-nociceptive effects of acetylcholine due to its accumulation, resulting prolongation of nerve block with hemodynamic stability.

We hypothesized that peripheral nerve block with isobaric 0.25% bupivacaine and Fentanyl would be comparable to isobaric 0.25% bupivacaine and Neostigmine for the efficacy of anesthesia and analgesia, and in addition would provide a better postoperative recovery profile and readiness for discharge.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

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

入选标准

  • PATIENTS POSTED FOR UPPER LIMB FRACTURE SURGERIES OF PROBALE DURATION OF 2 HOURS ASA I & II.

排除标准

  • PATIENTS REFUSAL ALLERGY TO LOCAL ANAESTHETICS & USED ADJUVENTS LOCAL SITE INFECTION NEURODEGENERATIVE DISORDERS IN UPPER LIMB BLEEDING COAGULOPATHY PATIENT WITH HEPATIC & RENAL DISORDERS.

结局指标

主要结局

DURATION OF ANALGESIA

时间窗: AFTER 2 HOUR EVERY 10 MIN POSTOPERATIVELY

次要结局

  • DURATION OF SENSORY AND MOTOR BLOCK(AFTER 2 HOUR EVERY 10 MIN POSTOPERATIVELY)

研究者

申办方类型
Other [NOT APPLICABLE ]

研究点 (1)

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