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临床试验/CTRI/2025/09/094211
CTRI/2025/09/094211尚未招募4 期

Randomized double-blind controlled trial comparing the analgesic effect of Dexamethasone versus Clonidine as adjuvants to 0.5% Levobupivacaine in ultrasound-guided supraclavicular brachial plexus block in patients undergoing upper limb surgery at SMS Medical College, Jaipur.”

SMS Medical College Jaipur1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年11月1日最近更新:
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试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
66
试验地点
1
主要终点
Duration of analgesia: Time from block administration to first rescue analgesia (minutes)

研究概览

简要总结

A prospective randomized double blind clinical study to compare the analgesic and anesthetic efficacy of Dexamethasone versus Clonidine as adjuvents to 0.5% Levobupivacain in ultrasound guided supraclavicular brachial plexus block in patients undergoing upper limb surgery. Primary outcome is total dural of analgesia, with secondary outcomes  including onset/duration of sensory and motor block,hemodynamic changes and adverse events.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

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

入选标准

  • •ASA physical status I or II Weight 50–80 kg Patients undergoing upper limb surgery under supraclavicular block Written informed consent provided.

排除标准

  • •Allergy to study drugs (local anesthetic, dexamethasone, clonidine) Coagulopathy or anticoagulant therapy Local infection at injection site Psychiatric illness or anxiety Respiratory illness/compromise Peripheral neuropathy or suspected compartment syndrome Participation in another trial.

结局指标

主要结局

Duration of analgesia: Time from block administration to first rescue analgesia (minutes)

时间窗: Continuously monitored postoperatively; recorded up to 24 hours after block

次要结局

  • Onset of sensory block(Time Point: Assessed at 0, 2, 5, 10, 15, 20, and 30 minutes after block administration)
  • Duration of sensory block(Monitored until regression; recorded up to 24 hours postoperatively)
  • Onset of motor block(Assessed at 0, 10, 20, and 30 minutes after block administration)
  • Duration of motor block(Monitored until regression; recorded up to 24 hours postoperatively)
  • Adverse effects(Intraoperative and up to 24 hours postoperatively)

研究者

发起方
SMS Medical College Jaipur
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Payal Mittal

Department of Anaesthesiology and Critical Care, SMS Medical College & Attached Hospitals, Jaipur

研究点 (1)

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