跳至主要内容
临床试验/CTRI/2024/11/076919
CTRI/2024/11/076919尚未招募不适用

A comparative study of isobaric ropivacaine with clonidine and isobaric ropivacaine alone in supraclavicular brachial plexus block

Dr Nameirakpam Priyadarshini Devi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年11月30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
100
试验地点
1
主要终点
To compare the dose response relationship between isobaric ropivacaine with clonidine and isobaric ropivacaine alone regarding anaesthesia quality and duration

研究概览

简要总结

The study explores the efficacy of isobaric ropivacaine alone versus isobaric ropivacaine combined with clonidine in supraclavicular brachial plexus blocks for upper extremity surgeries

brachial plexus blocks offer advantages over general anesthesia including reduced risks better pain relief and fewer complications like nausea and vomiting

ropivacaine a local anesthetic works by blocking sodium channels to inhibit nerve impulse conduction selectively targeting pain transmitting fibers with less motor block

clonidine when added to ropivacaine enhances the nerve block by modulating adrenergic pathways leading to prolonged sensory blockade and reduced postoperative pain

the study aims to compare these two approaches to determine which provides better motor blockade longer duration of anesthesia, and improved postoperative pain management

4o mini

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • ASA physical status I II scheduled for elective upper limb orthopaedic surgeries under supraclavicular brachial plexus block.

排除标准

  • Lack of patients consent any other comorbidities COPD IHD HTN DM Renal or hepatic dysfunction etc patients with a known contraindication to any of the study drugs.

结局指标

主要结局

To compare the dose response relationship between isobaric ropivacaine with clonidine and isobaric ropivacaine alone regarding anaesthesia quality and duration

时间窗: every 5 minutes for 30 minutes every 30 minutes during the surgery and every hourly for 12 hours

次要结局

  • to evaluate whether the addition of clonidine improves pain management reduce the need for opioids and prolongs the duration of analgesia(every 5 minutes for 30 minutes every 30 minutes during the surgery and every hourly for 12 hours)

研究者

发起方
Dr Nameirakpam Priyadarshini Devi
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Nameirakpam Priyadarshini Devi

Varun Arjun Medical College and Rohilkhand Hospital

研究点 (1)

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