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临床试验/CTRI/2026/01/102462
CTRI/2026/01/102462尚未招募4 期

Ultrasound guided Supraclavicular block : Comparison of efficacy between Ropivacaine(0.5%) with fentanyl and Bupivacaine (0.5%) with fentanyl in upper limb surgeries

Dr Harshavarthini M1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年2月16日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

This study aims to evaluate the effectiveness and safety of the proposed intervention in improving perioperative outcomes among patients undergoing surgery under anaesthesia. Eligible participants will be recruited based on predefined inclusion and exclusion criteria after obtaining informed consent. The study will follow an appropriate observational/interventional design with systematic data collection on demographic variables, clinical parameters, and outcome measures. Standard anaesthetic and monitoring protocols will be adhered to throughout the study period. Data will be analyzed using suitable statistical methods to assess primary and secondary outcomes. The findings are expected to contribute valuable evidence to improve anaesthetic management and patient safety in clinical practice.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patient consent to participate in the study Age 18-65 years ASA physical status I and II Elective upper limb surgeries under supraclavicular block.

排除标准

  • Patient refusal to participate in the study Coagulopathy Allergy to study drugs Infection at injection site Pregnancy/lactation Neurological or psychiatric disorders.

研究者

发起方
Dr Harshavarthini M
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Harshavarthini M

Vinayaka Missions Kirupananda Variyar Medical college and hospital

研究点 (1)

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